A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657046



Internal ID9923151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133177190..133177535hg38UCSC Ensembl
Outerchr10:133177151..133177592hg38UCSC Ensembl
Innerchr10:134990694..134991039hg19UCSC Ensembl
Outerchr10:134990655..134991096hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6043364, essv6377171, essv5439645, essv6114003, essv5933373, essv6414606, essv5894915, essv5453561, essv6350794, essv6588480, essv5919741, essv5712691, essv6253740, essv6053069, essv6251762, essv6445408, essv5614922, essv6262313, essv6164490, essv5901958, essv5819071, essv5729577, essv5909026, essv6295981, essv6104143, essv6047821, essv6275861, essv5609639, essv5868154, essv6552906, essv5462034, essv6494831, essv5727469, essv5739612, essv6419568, essv6230023, essv6575494, essv5874356, essv5469882, essv5452798, essv5937370, essv6401785, essv6245488, essv6074744, essv6052660, essv5442580, essv5876758, essv5945532, essv5797633, essv5983922, essv6542210, essv6231475, essv6575643, essv6182514, essv5658256, essv5953158, essv6207540, essv6008339, essv5975699, essv6344685, essv6304911, essv5596918, essv6281381, essv5811289, essv6339988, essv6316960, essv5616605, essv5626266, essv6045909, essv6560061, essv5436226, essv5732316, essv5933759, essv6115059, essv6358200, essv6373878, essv6318599, essv5898023, essv6154147, essv5883057, essv6263835, essv5633591, essv6188459, essv5418118, essv5920137, essv5807877, essv5721914, essv6380964, essv6127060, essv5634873, essv6421326, essv5828203, essv5685477, essv5463452, essv5810302, essv6289184, essv5701657, essv5775099, essv6547007, essv5477460, essv5400865, essv5497903, essv5951843, essv5994695, essv6182880, essv6043591, essv5893800, essv6220959, essv5688425, essv6530077, essv5635827, essv6357404, essv6368622, essv5622302, essv5572162, essv6395463, essv5544954, essv5585656, essv6532184, essv6253062, essv6458901, essv5958653, essv5729537, essv6165246, essv5879656, essv6284638, essv5871939, essv5980437, essv6162438, essv6475585, essv6236988, essv5422357, essv6515970, essv5961310, essv6440761, essv5528189, essv5606286, essv6329417
SamplesNA20588, NA12717, HG00442, NA11830, NA20529, NA12842, NA18621, HG00142, NA20766, NA18861, NA18592, NA18508, NA10851, HG00524, NA18980, NA20514, NA18561, NA12843, NA11931, NA18599, HG00315, HG00306, NA20816, NA20813, NA18603, NA18545, NA20805, NA18596, NA18530, NA18606, NA20808, NA20507, NA19190, NA20771, NA12413, NA20814, NA18563, NA18940, HG01070, HG00589, NA18597, NA20798, NA18595, NA18635, NA20756, NA20795, NA12348, NA18942, NA20768, NA20540, HG00369, NA20513, NA18964, NA18949, HG00281, NA20759, NA19720, NA20518, NA20775, NA11932, NA18986, NA12889, HG00427, NA20811, HG00323, HG00253, NA20515, NA20755, NA18638, NA10847, NA12489, NA20800, HG00443, HG00268, NA20787, NA20810, NA20536, HG00556, NA20519, NA18948, NA18548, HG00284, NA18573, NA19084, NA20581, HG00525, NA12827, HG00146, NA20828, NA20542, NA18858, NA12546, NA18945, NA19012, NA20799, NA18632, HG00476, NA20773, HG00155, HG00119, NA12775, NA20815, NA18950, HG00136, NA20804, NA20520, NA07051, NA12046, NA20530, HG00308, NA20778, NA20544, HG00116, NA18943, NA20803, HG00256, NA19783, HG00513, NA20582, NA18636, NA12830, NA20786, NA20807, NA20758, NA20826, NA20528, NA18552, NA20502, NA12006, NA07000, NA20585, NA18612, NA18549, NA20754, NA18965, NA20772, NA20509, NA18620
Known GenesKNDC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657046
Frequency
Sample Size1151
Observed Gain0
Observed Loss138
Observed Complex0
Frequencyn/a


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