A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669356



Internal ID9935461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26554059..26554480hg38UCSC Ensembl
chr18:24134023..24134444hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5523265, essv6508249, essv6414003, essv6324021, essv5443043, essv5701205, essv6440811, essv5834287, essv6014811, essv5911200, essv6476767, essv5842777, essv5457422, essv5633835, essv5803821, essv5880250, essv5401591, essv6446380, essv6282601, essv6273957, essv6503199, essv5577279, essv6221965, essv5718288, essv5885391, essv5758245, essv5673680, essv5788460, essv5486110, essv6525613, essv5483195, essv5486495, essv5968183, essv6378300, essv6576951, essv5887094, essv6147260, essv5795127, essv5632996, essv5988232, essv6034345, essv6574600, essv5826812, essv5685928, essv6319577, essv6507429, essv6425102, essv6327035, essv5702399, essv5874934, essv6483441, essv5862018, essv5527049, essv5426590, essv6483021, essv5396178, essv5457867, essv5960001, essv6065338, essv5681717, essv5676184, essv5542036, essv5515192, essv6538431, essv6170095, essv6258570, essv5947906, essv6100386, essv5866812, essv6249218, essv6064486, essv5542393, essv6590692, essv5657590, essv6277264, essv5939046, essv5397830, essv5411064, essv6571400, essv5800814, essv5777707, essv5697004, essv5636805, essv5896288, essv5405529, essv6052190, essv6142961, essv6221283, essv6426420, essv5467682, essv6163750, essv6400407, essv6021856, essv5644409, essv5863200, essv6537140, essv5896463, essv6381467, essv6122606, essv6516682, essv5915622, essv5575234, essv6148454, essv6530731, essv6141266, essv5801351, essv5839068, essv6541038, essv6493920, essv6290201, essv5609537, essv5957656, essv6309928, essv6540830, essv5446055, essv5798419, essv6406024, essv6547486, essv6072222, essv6246836, essv5440485, essv6022528, essv6153521
SamplesHG00626, HG00650, HG00442, HG01173, NA19058, HG00592, HG00231, NA18621, NA19066, HG00187, NA12843, NA11933, HG00318, HG00699, NA18596, NA18616, NA20517, NA12750, NA18602, HG00693, NA18988, NA18627, NA12341, NA07346, NA18940, NA18550, HG01070, HG00589, NA18597, HG00689, HG00173, NA18982, NA20317, NA18619, NA18558, HG01492, NA18960, NA19062, HG00346, HG00185, NA19904, NA18949, HG00590, NA11930, HG00325, NA18560, HG00534, NA19075, NA19385, NA19002, NA18557, HG00323, NA18973, HG01550, HG00419, NA19789, NA18539, HG00464, HG00543, NA18613, HG00443, HG01360, NA19070, HG00557, HG00190, NA20809, HG00701, HG00657, HG00436, NA18637, HG00500, NA18534, HG00708, NA11919, HG00651, HG00690, HG00531, HG00331, NA11894, NA06989, HG00613, HG00525, NA18553, HG01334, NA18963, HG00704, NA12144, NA18953, NA19003, HG00258, HG00336, NA18564, NA18941, HG00278, NA19083, NA18943, NA20797, NA07037, HG00256, HG00418, NA18615, HG00578, NA19060, HG00329, NA12749, HG01055, HG00123, HG00186, HG00112, HG00698, NA18552, HG00372, NA18984, NA18989, NA19004, HG00628, NA18623, NA19065, HG01112, NA18612, HG00180, NA18622, NA18965
Known GenesKCTD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669356
Frequency
Sample Size1151
Observed Gain0
Observed Loss123
Observed Complex0
Frequencyn/a


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