A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611580



Internal ID6651798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163515945..163524558hg38UCSC Ensembl
Innerchr6:163515945..163524558hg38UCSC Ensembl
Outerchr6:163515597..163524863hg38UCSC Ensembl
chr6:163936977..163945590hg19UCSC Ensembl
Innerchr6:163936977..163945590hg19UCSC Ensembl
Outerchr6:163936629..163945895hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg388614
hg198614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12625325, essv12625327, essv12625326, essv12625329, essv12625330, essv12625328, essv12625324
SamplesHG01606, HG00256, HG01702, HG01779, NA20799, HG00379, HG01781
Known GenesQKI
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611580
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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