A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611578



Internal ID6651796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163497743..163522920hg38UCSC Ensembl
Innerchr6:163497770..163522894hg38UCSC Ensembl
Outerchr6:163497717..163522947hg38UCSC Ensembl
chr6:163918775..163943952hg19UCSC Ensembl
Innerchr6:163918802..163943926hg19UCSC Ensembl
Outerchr6:163918749..163943979hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3825178
hg1925178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12625316, essv12625313, essv12625312, essv12625314, essv12625315, essv12625311
SamplesHG01779, HG01702, HG00379, NA20799, HG01606, HG01781
Known GenesQKI
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611578
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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