A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676051



Internal ID9942156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33747322..33747643hg38UCSC Ensembl
chr20:32335128..32335449hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6053990, essv6172277, essv6480806, essv5423156, essv6160122, essv6330027, essv6465587, essv5686858, essv5730598, essv5849176, essv6480690, essv6259285, essv5512755, essv6359012, essv6294528, essv5517584, essv5451189, essv5590870, essv5834071, essv5413825, essv5719673, essv5501183, essv6440127, essv5795566, essv5722454, essv5759873, essv5678567, essv6107687, essv6516024, essv5598982, essv6047626, essv5999351, essv5696175, essv6322191, essv5816468, essv5658864, essv6494774, essv6165198, essv5669109, essv5776050, essv5911511, essv5683081, essv6483054, essv5492184, essv6399904, essv5436636, essv5885848, essv5951600, essv6020223, essv5748622, essv5755399, essv6294038, essv5737128, essv5552964, essv6490756, essv6596261, essv6492126, essv5396007, essv6005417, essv5809867, essv5970222, essv5497040, essv5817705, essv5682652, essv6536712, essv5813787, essv5414246, essv5625763, essv5596515, essv5788658, essv5866969, essv6202424, essv6290428, essv6060299, essv5555158, essv5577422, essv5726995, essv6448290, essv5944968, essv6179860, essv6393343, essv5983674, essv5720007, essv6337262, essv6265996, essv5935591, essv6420952, essv5669332, essv5734357, essv5778892, essv5689807, essv5567302, essv6201888, essv6464078, essv5843479, essv5735706, essv5856687, essv6127712, essv5461503, essv5618112, essv6307660, essv5585628, essv6177061, essv6031947, essv6407285, essv6424363, essv6174505, essv5931822, essv5669336, essv6078015, essv6073166, essv5536654, essv6315558, essv5965895, essv6230045, essv5721792, essv6041745, essv5962639, essv6425348, essv6346848, essv6009217, essv5908535, essv6477404, essv6215577, essv5901406, essv5552775, essv5778357
SamplesNA19394, NA18502, NA19701, NA19700, NA19703, NA19397, NA11829, NA19204, NA12414, NA18561, NA19704, NA18507, HG01188, NA19350, NA19359, NA20294, NA19355, NA19819, NA12004, NA19377, NA20346, NA19098, NA18870, NA19920, NA18510, NA12813, NA19446, NA18967, NA19374, NA19373, NA19171, NA18519, NA18489, NA19119, NA19198, NA19131, NA18942, NA19457, NA19138, NA18498, NA19904, NA19384, NA19404, NA19720, NA19383, NA19917, NA19137, NA19371, NA19238, NA11994, NA19235, NA19207, NA19385, NA19172, NA19471, NA19317, NA19159, NA19239, NA19209, NA18975, NA18908, NA19451, NA19200, NA11831, NA19210, NA19437, HG01360, NA19707, NA19403, NA12003, NA19462, NA19347, NA19152, NA18956, NA19391, NA19455, NA19236, NA18516, NA19982, NA18910, NA18871, NA18976, NA18981, HG01094, NA20299, NA11894, NA18856, NA18912, NA18853, NA19452, NA19225, NA19469, NA19318, NA19160, NA19625, HG01107, NA18974, NA18953, NA19440, NA12716, NA19390, NA11881, NA19834, NA19108, NA19147, NA19240, NA19144, NA19439, NA19470, NA19311, NA19467, NA18943, NA20281, NA19818, NA19223, NA19474, NA19102, NA18873, HG01125, NA19463, NA18511, NA18522, HG00554, NA19429, NA19346, NA18487, NA12776
Known GenesZNF341
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676051
Frequency
Sample Size1151
Observed Gain0
Observed Loss127
Observed Complex0
Frequencyn/a


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