A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2678346

Internal ID9597765
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35360514..35372120hg38UCSC Ensembl
Outerchr19:35360143..35372590hg38UCSC Ensembl
Innerchr19:35851416..35863022hg19UCSC Ensembl
Outerchr19:35851045..35863492hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv637e199
Supporting Variantsessv5837706, essv6173345, essv5795262, essv5713996, essv5618041, essv6477700, essv5828853, essv5647654, essv5621912, essv6048394, essv6131018, essv6350732, essv6535008, essv6203280, essv5950747, essv5912100, essv5631259, essv6575668, essv6511946, essv5985611, essv6465475, essv5490058, essv6136499, essv6091402, essv5917777, essv5715467, essv6446476, essv5934946, essv5891782, essv6081557, essv6312277, essv5475816, essv5519160, essv6466875, essv6254122, essv5942301, essv6177978, essv5773241, essv5447267, essv6539451, essv5921569, essv5607210, essv6485047, essv6541498, essv5408572, essv5868474, essv6340218, essv5932784, essv5799027, essv6141602, essv6185992, essv6491409, essv6262381, essv5792755, essv6321955, essv5931795, essv5579401, essv6195460, essv5401551, essv5428286, essv5741950, essv6592132, essv6416194, essv5452359, essv5725876, essv6079034, essv6419942, essv5846302, essv6013837, essv5768964, essv6188085, essv5570382, essv6543581, essv6289591, essv5563960, essv5712221, essv6129230, essv6102441, essv6382815, essv5410744, essv5832905, essv6263657, essv6325866, essv6105233, essv6553442, essv5947210, essv5585640, essv6250694, essv6094651, essv5914967, essv6322803, essv5571455, essv6233346, essv5957300, essv6161240, essv6531703, essv5484816, essv5627745, essv6538507, essv6119306, essv5733876, essv6567428, essv5900746, essv6200862, essv5784731, essv6469161, essv5395871, essv5504557, essv5571221, essv6098602, essv5791371, essv6330075, essv5755660, essv5556194, essv5687204, essv5499612, essv5781844, essv6192664, essv6245506, essv6326147, essv5929263, essv5548637, essv6502998, essv5585189, essv6083261, essv5882124, essv6414133, essv5800378, essv6545901, essv6578761
SamplesHG00323, HG00613, HG00309, NA12154, NA12249, HG00607, NA12750, NA07037, NA18951, HG00344, NA12342, HG00328, NA18975, HG00171, HG00596, NA12347, HG00449, NA19060, HG00310, NA19003, HG00707, NA10847, NA12340, NA18948, HG00657, HG00577, NA18953, NA18972, NA12828, HG00428, NA19010, HG00542, HG00326, HG00701, NA12776, HG00187, HG00651, HG00366, NA11893, HG00177, NA12341, NA12287, NA18943, HG00353, NA19062, HG00321, NA18967, NA19059, NA12282, NA12383, HG00337, NA11994, NA18960, HG00610, HG00692, HG00689, HG00628, HG00330, NA07048, NA12761, NA19066, HG00178, HG00419, NA11843, NA11831, NA11894, NA19075, NA11995, HG00174, HG00276, NA12777, HG00343, NA12144, NA19082, NA12751, HG00436, HG00267, HG00620, NA19080, NA12046, NA12716, HG00268, NA12778, NA18968, NA12275, NA19002, NA18941, HG00478, NA18961, HG00513, NA18988, HG00512, HG00534, NA12283, NA18985, NA18940, NA11832, NA18987, HG00590, HG00595, NA12272, HG00443, NA19078, NA06984, NA12413, NA19009, HG00663, HG00530, NA11992, NA12003, NA19064, HG00281, HG00285, NA12399, HG00656, HG00367, NA12045, NA11932, HG00566, HG00320, HG00275, HG00690, NA12717, HG00684, NA06994, HG00336, HG00704, HG00271, NA19007, HG00327
Known GenesFFAR3
AnalysisNo reference, merging analysis
CommentsHigh quality site
Pubmed ID23128226
Accession Number(s)esv2678346
Sample Size1151
Observed Gain0
Observed Loss130
Observed Complex0

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