A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676545



Internal ID9942650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8023953..8025355hg38UCSC Ensembl
chr10:8065916..8067318hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381403
hg191403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv117e199
Supporting Variantsessv6273026, essv6305892, essv6305453, essv6343457, essv6472295, essv5569214, essv6021364, essv5545038, essv6107138, essv5433736, essv6561186, essv6035682, essv6259424, essv5647406, essv6184619, essv5683986, essv6315415, essv6593400, essv6170999, essv6380562, essv5845818, essv5538507, essv5484844, essv6343757, essv5598834, essv6340452, essv6026517, essv6113077, essv6498772, essv5654064, essv6330679, essv6476676, essv6111730, essv5619275, essv5549332, essv5935615, essv6075178, essv5876296, essv6378770, essv6067819, essv5596122, essv6039661, essv5878362, essv6164765, essv5594799, essv6048458, essv6353856, essv6103573, essv6505820, essv6428971, essv5585852, essv6341221, essv5817719, essv5621516, essv6314807, essv5709104, essv5727907, essv5771582, essv5784204, essv6130246, essv6292187, essv6101905, essv6151786, essv5744214, essv6409729, essv5689580, essv5855191, essv5631570, essv5567899, essv5754279, essv5720185
SamplesNA19701, HG00442, NA19058, NA18924, HG01462, HG00608, NA19909, NA19399, NA19914, NA19704, NA18917, NA19350, NA19777, NA20332, NA20346, NA19443, NA19190, NA12400, NA18988, NA18571, NA18977, NA18868, NA20340, NA19371, NA19235, NA19471, HG00705, NA18986, NA19087, NA19002, NA19901, NA19985, HG00264, NA20818, NA19908, NA19056, NA18933, HG00533, NA18871, NA20344, NA11919, NA19084, HG00404, NA11893, NA19452, HG00463, HG00246, NA19003, NA19440, NA18533, NA19321, NA19473, NA19380, HG01357, NA19818, HG00578, NA19474, NA18873, NA19780, NA19213, NA19900, HG01378, NA18488, HG01111, HG01082, NA19312, HG01125, NA18623, NA18522, NA19429, NA18620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676545
Frequency
Sample Size1151
Observed Gain0
Observed Loss71
Observed Complex0
Frequencyn/a


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