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11:63991801 T / C


Filter Status
PASS
dbSNP
rs1059440
Allele Frequency
0.1698
Filtering AF
0.2999 (Latino)
Allele Count
20517 / 120860
UCSC
11-63991801-T-C
ClinVar
Click to search for variant in Clinvar
Note: Plot may include low-quality genotypes that were excluded from allele counts in the table above

Note: These are site-level quality metrics: they may be unpredictable for multi-allelic sites.

Population Frequencies
Population Allele Count Allele Number Number of Homozygotes Allele Frequency
European (Non-Finnish) 11331 66370 996 0.1707
East Asian 1618 8598 147 0.1882
Other 170 902 15 0.1885
African 1084 10336 51 0.1049
Latino 3559 11542 576 0.3084
South Asian 1608 16500 99 0.09745
European (Finnish) 1147 6612 100 0.1735
Total 20517 120860 1984 0.1698

Read Data

This interactive IGV.js visualization shows reads that went into calling this variant.
Note: These are reassembled reads produced by GATK HaplotypeCaller --bamOutput so they accurately represent what HaplotypeCaller was seeing when it called this variant.