Genotyping and Sequencing Data

1000 Genomes Sequencing Data (includes CEU samples (Utah residents with Northern and Western European ancestry from the CEPH collection)):

Whole-Genome Sequencing Data (available for some CEPH, some Yoruba, some Puerto Rican, and some diversity populations):

Centre d'Etude du Polymorphisme Humain (CEPH) Genotyping Data:

*The 1000 Genomes Browser http://www.ncbi.nlm.nih.gov/variation/tools/1000genomes/ hosted by NCBI provides access to variant calls, genotype calls, and supporting sequence read alignments produced by the 1000 Genomes project. With the 1000 Genomes Browser, users can access genotype data from either the Phase 3 or Phase 1 call sets. The browser displays the Phase 3 data by default, but users can access Phase 1 data by clicking on the banner at the top of the browser. Information about Coriell samples can be found under the column heading “Populations / Samples”. To search for specific variants, users can use the “Search” widget located below the “Ideogram View” widget on the left. The Search widget will accept a location directive, such as chr1:1,500,000-2,000,000 or a search term (such as 'PTEN' or 'rs13432'). The Genotype table provides access to individual level genotypes and population allele frequencies. Rows display information about populations and individuals, while columns display information about variants. To see individual level genotypes, click on the arrow next to the population abbreviation and it will open to display the genotypes of individuals from that population. The reference allele is always displayed first. The most frequent allele is always bolded.