The population density of Anchorage Municipality, AK was 174 in 2018.

Population Density

Population Density is computed by dividing the total population by Land Area Per Square Mile.

Above charts are based on data from the U.S. Census American Community Survey | ODN Dataset | API - Notes:

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Geographic and Population Datasets Involving Anchorage Municipality, AK

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    CAMA Property Inventory - Residential and Commercial Combined | Last Updated 2022-01-19T08:31:23.000Z

    All properties in the Municipality of Anchorage including data elements that are common to both residential and commercial properties. Disclaimer This is unofficial, unaudited data that is subject to revision. This data may contain minor errors or discrepancies not present in official, audited data and reports. This data is intended as a starting point for citizens and researchers to begin their exploration of the Municipality of Anchorage’s property and valuation data.

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    [ARCHIVED] Census Population Density | Last Updated 2020-01-06T15:04:30.000Z

    <b>[ARCHIVED]</b> Community Counts data is retained for archival purposes only, such as research, reference and record-keeping. This data has not been maintained or updated. Users looking for the latest information should refer to Statistics Canada’s Census Program ( for the latest data, including detailed results about Nova Scotia. This table reports population density. This data is sourced from the Census of Population. Geographies available: provinces, counties, communities, municipalities, district health authorities, community health boards, economic regions, police districts, school boards, municipal electoral districts, provincial electoral districts, federal electoral districts, regional development authorities, watersheds

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    Real Property Assessment Equity Statistics By Municipality: Beginning 2004 | Last Updated 2021-12-31T17:28:08.000Z

    The Department of Taxation and Finance annually produces a report documenting the results of the Market Value Survey pertaining to property assessment. The report contains the staff findings regarding assessment equity by municipality in New York State, that is, the degree to which assessments are at a uniform percentage of their market value. Equity is measured primarily by two statistics — the coefficient of dispersion (COD) and the price-related differential (PRD). For more information please go to:

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    USDA FoodEnvironmentAtlas - Socioeconomic Characteristics | Last Updated 2021-09-22T11:59:02.000Z

    This dataset contains Socioeconomic Characteristics metrics displayed in the <a href="" target="_blank">U.S. Department of Agriculture (USDA) Food Environment Atlas website</a>, including County resident population by groupings of humans based on shared physical or social qualities into categories generally viewed as distinct by society. Data was last updated on the USDA website in September 2020. Any data elements with numerical values reflect figures at the locality-level unless otherwise specified with an asterisk (*). See column descriptions for details. For more information on all metrics in this dataset, see the <a href="" target="_blank">Food Environment Atlas Socioeconomic Characteristics documentation</a>.

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    NCHS - Teen Birth Rates for Females by Age Group, Race, and Hispanic Origin: United States | Last Updated 2020-06-05T17:24:48.000Z

    This dataset includes teen birth rates for females by age group, race, and Hispanic origin in the United States since 1960. Data availability varies by race and ethnicity groups. All birth data by race before 1980 are based on race of the child. Since 1980, birth data by race are based on race of the mother. For race, data are available for Black and White births since 1960, and for American Indians/Alaska Native and Asian/Pacific Islander births since 1980. Data on Hispanic origin are available since 1989. Teen birth rates for specific racial and ethnic categories are also available since 1989. From 2003 through 2015, the birth data by race were based on the “bridged” race categories (5). Starting in 2016, the race categories for reporting birth data changed; the new race and Hispanic origin categories are: Non-Hispanic, Single Race White; Non-Hispanic, Single Race Black; Non-Hispanic, Single Race American Indian/Alaska Native; Non-Hispanic, Single Race Asian; and, Non-Hispanic, Single Race Native Hawaiian/Pacific Islander (5,6). Birth data by the prior, “bridged” race (and Hispanic origin) categories are included through 2018 for comparison. National data on births by Hispanic origin exclude data for Louisiana, New Hampshire, and Oklahoma in 1989; New Hampshire and Oklahoma in 1990; and New Hampshire in 1991 and 1992. Birth and fertility rates for the Central and South American population includes other and unknown Hispanic. Information on reporting Hispanic origin is detailed in the Technical Appendix for the 1999 public-use natality data file (see SOURCES NCHS, National Vital Statistics System, birth data (see; public-use data files (see; and CDC WONDER (see REFERENCES 1. National Office of Vital Statistics. Vital Statistics of the United States, 1950, Volume I. 1954. Available from: 2. Hetzel AM. U.S. vital statistics system: major activities and developments, 1950-95. National Center for Health Statistics. 1997. Available from: 3. National Center for Health Statistics. Vital Statistics of the United States, 1967, Volume I–Natality. 1969. Available from: 4. Martin JA, Hamilton BE, Osterman MJK, et al. Births: Final data for 2015. National vital statistics reports; vol 66 no 1. Hyattsville, MD: National Center for Health Statistics. 2017. Available from: 5. Martin JA, Hamilton BE, Osterman MJK, Driscoll AK, Drake P. Births: Final data for 2016. National Vital Statistics Reports; vol 67 no 1. Hyattsville, MD: National Center for Health Statistics. 2018. Available from: 6. Martin JA, Hamilton BE, Osterman MJK, Driscoll AK, Births: Final data for 2018. National vital statistics reports; vol 68 no 13. Hyattsville, MD: National Center for Health Statistics. 2019. Available from:

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    AFSC/ABL: 1996 Brood year Steelhead growth and early life-history transitions | Last Updated 2017-09-19T04:57:22.000Z

    Heritabilities of growth, precocious maturation and smolting were measured in 75 families of juvenile steelhead or rainbow trout Oncorhynchus mykiss, progeny of within and between line matings (crosses) of wild, anadromous steelhead and wild, resident (lake) rainbow trout originally derived from the same anadromous stock 70 years earlier. The tagged yearling progeny were combined by line in common freshwater rearing containers and graded into three categories: mature, smolt or rearing (undifferentiated) at age 2 years. Heritabilities of precocious male maturity, smolting and growth were moderate to high, and the genetic correlation between growth and smolting was low. Smolting and precocious male maturity were highly variable among families within lines and significantly different between lines. Each of the four lines produced significant numbers of smolts at age two. Smolting and maturation were negatively genetically correlated, which may explain the persistence of smolting in the lake population despite strong selection against lake smolts; balancing selection on male maturation age may help to maintain variation for smolting. The high heritability of smolting, coupled with the inability of smolts that leave the lake to return to it indicates that the genetic potential for smolting can lie dormant or be maintained through a dynamic interaction between smolting and early maturation for decades despite complete selection against the phenotype. The results have significant implications for the preservation of threatened anadromous stocks in fresh water and the inclusion of resident fish of formerly anadromous populations, currently trapped behind long-standing barriers to migration, as one component of the same population.

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    Municipality Breakdown | Last Updated 2019-02-15T21:07:02.000Z

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    AFSC/ABL: Sockeye salmon allozyme baseline - 1982-1990 | Last Updated 2017-09-19T04:56:56.000Z

    Genetic data were collected and prepared with the use of protein electrophoresis from 52 spawning locations in southeastern Alaska and northern British Columbia. Genetic relationships were examined from principal components analysis and unrooted trees constructed from genetic distances between collections. These descriptive analyses suggest a geographic basis to genetic divergence among populations. This geographic basis was confirmed using log-likelihood-ratio analysis and analyses of variance. Three groups of populations were observed: one from systems that drain into the inside waters of northern and central southeast Alaska; another from the far southeastern islands (including Prince of Wales Island); and the third in systems of the southern inside waters. Although the geographic structure was a statistically significant component of the overall genetic structure, gene diversity analysis indicates that only about 4.7% of the total genetic variability was attributable to genetic differences among those regions, whereas about 8.4% of the total was due to differences among populations within each region. The other 87.0% of the variation occurred, on average, within each collection.

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    Incidence Rate Of Mesothelioma Per 100,000 All States | Last Updated 2019-04-19T05:29:37.000Z

    Incidence Rate Of Mesothelioma Per 100,000 All States

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    Incidence Rate Of Pancreatic Cancer Per 100,000 All States | Last Updated 2019-04-19T06:47:25.000Z

    Incidence Rate Of Pancreatic Cancer Per 100,000 All States