A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622281



Internal ID7009140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8023935..8025356hg38UCSC Ensembl
Innerchr10:8023936..8025355hg38UCSC Ensembl
Outerchr10:8023934..8025357hg38UCSC Ensembl
chr10:8065898..8067319hg19UCSC Ensembl
Innerchr10:8065899..8067318hg19UCSC Ensembl
Outerchr10:8065897..8067320hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381422
hg191422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13690254, essv13690295, essv13690278, essv13690273, essv13690277, essv13690256, essv13690288, essv13690312, essv13690276, essv13690305, essv13690259, essv13690284, essv13690275, essv13690266, essv13690291, essv13690253, essv13690283, essv13690300, essv13690272, essv13690258, essv13690257, essv13690271, essv13690269, essv13690274, essv13690293, essv13690292, essv13690306, essv13690301, essv13690304, essv13690281, essv13690307, essv13690279, essv13690286, essv13690285, essv13690309, essv13690270, essv13690311, essv13690287, essv13690303, essv13690255, essv13690297, essv13690265, essv13690252, essv13690260, essv13690308, essv13690263, essv13690290, essv13690299, essv13690298, essv13690264, essv13690296, essv13690310, essv13690289, essv13690262, essv13690302, essv13690294, essv13690267, essv13690261, essv13690282, essv13690268, essv13690280
SamplesNA20339, HG03484, NA18924, HG02433, HG02419, NA18877, NA19350, HG03100, HG03295, NA20332, HG03518, HG03139, NA19443, NA19190, HG03099, NA19197, HG03224, HG03079, NA18868, HG03212, NA19235, HG02588, HG03352, NA19901, HG03073, NA19025, HG03270, HG02820, NA19908, HG02582, HG01162, NA19327, HG03457, NA18871, HG03388, HG02884, NA18853, HG03451, NA19452, HG02256, NA19160, HG01896, HG02772, NA19401, NA19149, HG02546, NA19454, NA19144, HG03565, HG03039, HG03112, HG02095, HG03066, HG03049, HG03279, NA19185, HG03351, HG02768, NA19096, HG01914, NA19429
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622281
Frequency
Sample Size2504
Observed Gain0
Observed Loss61
Observed Complex0
Frequencyn/a


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