A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678346



Internal ID9597765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35360514..35372120hg38UCSC Ensembl
Outerchr19:35360143..35372590hg38UCSC Ensembl
Innerchr19:35851416..35863022hg19UCSC Ensembl
Outerchr19:35851045..35863492hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812448
hg1912448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv637e199
Supporting Variantsessv6233346, essv5929263, essv5504557, essv6545901, essv5571221, essv6511946, essv5931795, essv5900746, essv5932784, essv5921569, essv6177978, essv6350732, essv6119306, essv6465475, essv6491409, essv5800378, essv5484816, essv6203280, essv6129230, essv5556194, essv6185992, essv5715467, essv5773241, essv6192664, essv5914967, essv6416194, essv5621912, essv5713996, essv5799027, essv5846302, essv6289591, essv6173345, essv5868474, essv6091402, essv5712221, essv5733876, essv5741950, essv5828853, essv6263657, essv6477700, essv6340218, essv6538507, essv5585640, essv5784731, essv5755660, essv5475816, essv5563960, essv5795262, essv5837706, essv5607210, essv6098602, essv5957300, essv6466875, essv6079034, essv6541498, essv6567428, essv5792755, essv5891782, essv6326147, essv5585189, essv6531703, essv5647654, essv5410744, essv5401551, essv6161240, essv6543581, essv5627745, essv6322803, essv5519160, essv5882124, essv6200862, essv5579401, essv6083261, essv6553442, essv5395871, essv6575668, essv5490058, essv6325866, essv5942301, essv6188085, essv5947210, essv5985611, essv5781844, essv6312277, essv6578761, essv6262381, essv6013837, essv5950747, essv5428286, essv6250694, essv6081557, essv6102441, essv6592132, essv5917777, essv5452359, essv6469161, essv6321955, essv6245506, essv5618041, essv6136499, essv5631259, essv6141602, essv6254122, essv6414133, essv5408572, essv6195460, essv5548637, essv6485047, essv6535008, essv5571455, essv5570382, essv6048394, essv5791371, essv6446476, essv6131018, essv5725876, essv5499612, essv6502998, essv6539451, essv5447267, essv6330075, essv6419942, essv5768964, essv5912100, essv5687204, essv6094651, essv6382815, essv6105233, essv5832905, essv5934946
SamplesNA12383, HG00542, NA12717, NA11995, NA19066, HG00187, NA12045, HG00367, NA12751, NA12340, HG00566, HG00449, HG00177, NA12750, NA12399, NA18988, NA12413, NA12341, HG00337, HG00327, HG00271, HG00663, NA18967, NA18940, HG00689, HG00330, NA18960, HG00610, NA19062, NA11992, NA07048, NA12283, NA12287, HG00590, NA12761, HG00512, HG00281, NA12282, NA12275, NA06984, NA11932, NA11994, HG00534, NA19075, HG00309, NA19002, NA18985, NA12828, NA18975, HG00326, HG00178, HG00323, HG00530, HG00419, NA19007, NA11831, NA10847, NA12777, NA18951, HG00443, HG00268, NA19082, HG00596, HG00328, NA12342, NA12003, HG00428, HG00577, HG00701, HG00657, HG00436, HG00320, HG00344, HG00275, NA18948, HG00692, NA19064, HG00651, HG00690, NA11893, NA11894, HG00684, NA12249, HG00613, HG00321, NA19059, NA19009, HG00276, HG00704, NA12144, NA12778, NA18953, NA19003, NA12716, HG00336, HG00285, NA18961, HG00366, HG00353, NA12272, NA18941, NA19010, NA12046, HG00607, NA18943, NA07037, NA12347, HG00620, NA19078, HG00707, NA06994, HG00513, HG00478, NA19060, NA18987, HG00656, HG00267, HG00174, HG00310, NA11843, NA19080, NA18972, HG00343, HG00595, HG00628, HG00171, NA18968, NA12154, NA12776, NA11832
Known GenesFFAR3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678346
Frequency
Sample Size1151
Observed Gain0
Observed Loss130
Observed Complex0
Frequencyn/a


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