A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670419



Internal ID9936524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:83432273..83432479hg38UCSC Ensembl
Outerchr11:83431902..83432849hg38UCSC Ensembl
Innerchr11:83143316..83143522hg19UCSC Ensembl
Outerchr11:83142945..83143892hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38948
hg19948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5603192, essv5593392, essv5469441, essv5857339, essv6472284, essv6261430, essv6576072, essv5513102, essv5829345, essv6046287, essv6453580, essv5825407, essv5744029, essv5603647, essv5979484, essv6014784, essv6523653, essv5786364, essv5886267, essv5424784, essv6192743, essv5560414, essv5731985, essv6584125, essv6285964, essv5747477, essv5860003, essv6455163, essv6478262, essv6136651, essv5829555, essv5571127, essv6508180, essv6113698, essv6176928, essv5486879, essv5701633, essv6541753, essv5977172, essv6178801, essv6463362, essv5401738, essv6491093, essv5924782, essv6106000, essv6384745, essv6289923, essv5519336, essv5667913, essv5872900, essv5565624, essv5818201, essv5645458, essv6209263, essv5608135, essv5930581, essv6308595, essv6053893, essv5450905, essv6126224, essv6433735, essv6478054, essv6241583, essv6036752, essv6078890, essv5819212, essv6587754, essv6551149, essv5852078, essv5707525, essv6417223, essv6492027, essv6083000, essv5550900, essv5492055, essv5988700
SamplesHG01441, HG01356, HG01462, NA19664, HG01359, HG01389, HG01374, HG01465, NA19684, HG01350, NA19728, HG01351, NA19678, HG01488, NA19723, HG01492, NA19771, HG01365, NA19782, NA19681, HG01134, NA19720, NA19651, NA19719, NA19731, NA19725, HG01550, NA19789, HG01353, HG01136, NA19657, NA19717, NA19663, HG01498, NA19788, NA19776, HG01390, NA19774, NA19655, HG01383, NA19750, HG01497, NA19761, NA19682, NA19675, HG01148, NA19729, NA19652, NA19749, NA19732, HG01551, HG01253, HG01357, HG01375, HG01494, NA19679, HG01113, HG01137, NA19783, HG01489, HG01342, NA19759, NA19785, HG01491, NA19779, NA19716, HG01254, HG01251, NA19661, HG01377, HG01378, NA19755, NA19758, HG01125, HG01437, NA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670419
Frequency
Sample Size1151
Observed Gain0
Observed Loss76
Observed Complex0
Frequencyn/a


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