A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611579



Internal ID6651797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163510682..163512107hg38UCSC Ensembl
Innerchr6:163510682..163512107hg38UCSC Ensembl
Outerchr6:163510582..163512163hg38UCSC Ensembl
chr6:163931714..163933139hg19UCSC Ensembl
Innerchr6:163931714..163933139hg19UCSC Ensembl
Outerchr6:163931614..163933195hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381426
hg191426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12625317, essv12625319, essv12625321, essv12625320, essv12625322, essv12625318, essv12625323
SamplesHG01606, HG03461, HG01702, HG01779, NA20799, HG00379, HG01781
Known GenesQKI
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611579
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer