A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673715



Internal ID9939820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32631939..32658045hg38UCSC Ensembl
Outerchr6:32631568..32658415hg38UCSC Ensembl
Innerchr6:32599716..32625822hg19UCSC Ensembl
Outerchr6:32599345..32626192hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3826848
hg1926848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5958926, essv5434274, essv5666203, essv5934987, essv5971291, essv6277475, essv6100170, essv6119464, essv5488186, essv6287188, essv6081796, essv6349500, essv5687623, essv6350799, essv6183555, essv5579399, essv5603938, essv6173208, essv5598502, essv6512132, essv6472277, essv5667086, essv5570575, essv6054656, essv6349753, essv6013899
SamplesNA19701, NA19703, NA19909, NA19914, NA19704, NA20294, NA20346, NA20356, NA19920, NA19916, NA20287, NA20340, NA19901, NA19985, NA19921, NA19707, NA20314, NA19982, NA20126, NA20344, NA20299, NA20282, NA20296, NA19712, NA19835, NA20334
Known GenesHLA-DQA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673715
Frequency
Sample Size1151
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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