The population genetics explorer

An atlas of
human genetic diversity.

Explore genetic distances among 319 populations, using data from 10,665 individuals drawn from a collection of published datasets and the Allen Ancient DNA Resource (AADR). Use the dropdowns to inspect any pair, or browse the nearest-population table for the selected reference group.

319populations
10,665individuals
302,955shared SNPs
50,721population pairs
Download Matrix TSV Download Long TSVDownload CSVPopulation sizesPopulation namesDiploid sensitivity CSVMethods and provenance
Explore the world

A world of genetic connections

Choose populations above, or use the buttons below to pick them on the map. Every coloured dot shows Fst relative to your reference.

Click a dot to choose the comparison population.
Select a marker to inspect its population.
Methods, estimation assumptions & sample filters

214 records have no heterozygous calls. The default counts these as one observed allele per site; this is an inferred ploidy assumption. Switch to the diploid analysis to inspect its effect. Only populations with at least 5 retained individuals are included. The threshold is applied after deduplication.

Buryat (41) and Mongol (9) are separate. Kalmyk (10) is also retained separately. Eight source-verified Tuscan individuals are labelled Tuscan. Duplicate and excluded records are omitted. Negative estimates are retained.

SNP coverage: Each SNP must have genotype calls in at least 80% of individuals and at least 5 individuals in each population being compared. Both estimation modes use the same coverage rule. Comparisons with fewer than 50,000 qualifying SNPs are unavailable on the map and in rankings; downloadable tables retain these estimates for audit.

Select two populations to view their Hudson's Fst.
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Population 1 N-
Population 2 N-
Observed SNPs-
Jackknife SE-

Nearest Populations To Population 1

Lowest Hudson's Fst first
Population N Hudson's Fst SE Observed SNPs

Population names. Expanded 1000 Genomes codes follow IGSR descriptions. Recruitment locations describe the original cohorts; approved pooled groups may include samples from additional locations. Data and methods. A collection of published datasets combined with present-day samples from AADR v66, including Inner Eurasian Human Origins and West Javanese data. All pairs recomputed on the shared marker panel after individual deduplication. Pair-specific SNP counts reflect missing data. SE uses a block jackknife; it does not capture label or inferred-ploidy uncertainty. Downloads contain the default adjusted estimates unless labelled diploid sensitivity. Hudson estimator: Bhatia et al. (2013); AADR: Mallick et al. (2024).