Interested in working on the development of this resource? Apply here.

11:6640007 C / CG


Filter Status
VQSRTrancheINDEL99.50to99.90
dbSNP
rs121908195
Allele Frequency
8.256e-06
Filtering AF
0 (None)
Allele Count
1 / 121130
UCSC
11-6640007-C-CG
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) 1 66588 0 1.502e-05
East Asian 0 8638 0 0
Other 0 906 0 0
African 0 10372 0 0
Latino 0 11542 0 0
South Asian 0 16504 0 0
European (Finnish) 0 6580 0 0
Total 1 121130 0 8.256e-06

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.