A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667003



Internal ID9933108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100398359..100399965hg38UCSC Ensembl
Outerchr10:100397988..100400335hg38UCSC Ensembl
Innerchr10:102158116..102159722hg19UCSC Ensembl
Outerchr10:102157745..102160092hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg382348
hg192348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5822066, essv5526590, essv6555936, essv5407070, essv6441891, essv5879228, essv5516283, essv6106896, essv5851655, essv5980298, essv5722509, essv6348555, essv5463909, essv5767475, essv5898570, essv5428610, essv6455569, essv5931643, essv6044457, essv5502159, essv6229534, essv5641948, essv5705290, essv5633620, essv5849416, essv6043159, essv6412280, essv5806092, essv5696212, essv6167440, essv5733068, essv6114172, essv6195993, essv6365367, essv6572917, essv5707849, essv6539091, essv5796729, essv5517675, essv6162172, essv5952825, essv5670575, essv5943412, essv6080054, essv6367935, essv6401155
SamplesHG00189, HG00361, HG00187, HG00315, HG00306, HG00367, HG00318, HG00181, HG00179, HG00337, HG00327, HG00271, HG00173, HG00330, HG00346, HG00369, HG00270, HG00185, HG00277, HG00325, HG00326, HG00178, HG00323, HG00188, HG00266, HG00183, HG00176, HG00328, HG00368, HG00344, HG00275, HG00324, HG00321, HG00276, HG00285, HG00353, HG00375, HG00278, HG00339, HG00329, HG00267, HG00310, HG00343, HG00274, HG00345, HG00180
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667003
Frequency
Sample Size1151
Observed Gain0
Observed Loss46
Observed Complex0
Frequencyn/a


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