A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668466



Internal ID9934571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145366128..145366291hg38UCSC Ensembl
chr7:145063221..145063384hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6420780, essv5654557, essv6296010, essv6196473, essv6043278, essv5689493, essv5740741, essv5952497, essv6280476, essv5835155, essv6386266, essv5413439, essv5936479, essv6116567, essv6034762, essv6570407, essv5812521, essv5465198, essv5704967, essv5965179, essv5754525, essv6332333, essv5552046, essv5606370, essv5640898, essv6313441, essv6265361, essv6433612, essv5868950, essv6279675, essv5885859, essv6342039, essv6158409, essv6205795, essv6592486, essv6272149, essv6242503, essv5410789, essv6259471, essv6395004, essv5995543, essv5997101, essv6412363, essv6089830, essv5565247, essv6105495, essv5885589, essv5809643, essv5961109, essv5915891, essv5798623, essv6159129, essv5513651, essv6147150, essv5760858, essv5952090, essv5931515, essv5724747, essv6483103, essv5627789, essv5405438, essv6304849, essv5857474, essv5540853, essv5826100, essv5731281, essv6366312, essv5442207, essv6512055, essv5424718, essv5982648, essv6059968, essv6349994, essv6033421, essv5525982, essv5497648, essv6522141, essv5487023, essv5756992, essv6438742, essv5835329, essv5679865, essv6231559, essv5587060, essv5821072, essv6580297, essv6005718, essv6218925, essv5493792, essv6229028, essv5630380, essv6086994, essv5892475, essv5624248, essv6040283, essv5632194, essv6042002, essv5932192, essv5610397, essv5489130, essv6390772, essv5906115, essv6196817, essv6509991, essv6562624, essv6194685, essv6077909, essv6329300, essv6423692, essv6008420, essv6350337, essv5977671, essv6036577, essv6070421, essv5984500, essv5619758, essv5639088, essv5709109, essv6233175, essv5990117, essv6014818, essv6101524, essv6512645, essv6083113, essv6404261, essv5830631, essv5966926, essv6037194, essv5491381, essv5982491, essv6334432, essv5499591, essv5940967, essv6383509, essv6106507, essv5747896, essv5708027, essv6316847, essv5506680, essv5832679, essv5892106, essv6301865, essv6472335, essv6115948, essv5995040, essv5774043, essv5688667, essv5885337, essv5871608, essv6115816, essv5452163, essv5565471, essv6073822, essv5866624, essv6314545, essv5671413, essv5746613, essv5653920, essv6426205, essv5623607, essv5406978, essv6122420, essv6098008, essv5567385, essv6566649, essv5692078, essv5683262, essv5816187, essv5518480, essv6330021, essv6080165, essv5905113, essv5592752, essv5438578, essv5987066, essv5865790, essv6509530, essv5656569, essv5883698, essv6553966, essv5948284, essv6369393, essv5642550, essv6109294, essv5852433, essv6113056, essv6254676, essv5753195, essv6474557, essv5977281, essv6268390, essv6271482, essv6055146, essv5699246, essv6414508, essv6376362, essv5785752, essv5943709, essv5720292, essv6243898, essv6226309, essv5412568, essv6073531, essv6417412, essv6375639, essv5563771, essv5546351, essv5862311, essv5656006
SamplesNA18502, NA20761, NA12717, HG00442, NA11830, HG00536, NA18924, NA20508, HG00671, NA19204, NA18861, NA12414, NA19704, NA18507, NA11920, NA11931, NA18599, HG01066, NA20816, HG00233, NA12045, NA19359, NA12004, NA19777, NA18504, NA20507, NA19190, NA19098, NA18870, NA18526, HG01051, NA18510, NA12155, NA07357, NA18602, HG00337, HG00271, NA12813, NA20537, NA18967, NA19374, NA19396, HG00138, NA19381, NA19171, NA18944, NA18940, NA18550, NA18519, NA19201, NA19382, HG01177, HG01488, NA19723, NA19119, NA19131, NA18960, NA18916, NA19197, HG00346, HG01354, NA18571, NA12287, HG01083, NA19138, NA18498, HG00158, NA12761, HG00277, HG01069, NA19651, HG01080, NA18874, NA20819, NA18868, HG00325, NA19917, NA19137, HG01072, HG00232, NA20340, NA19372, NA19371, NA19238, NA11994, NA19207, NA19385, NA19172, NA19159, NA20811, NA19189, HG00338, NA19209, NA18975, HG00326, HG00419, NA20515, NA20755, NA19921, NA18638, NA20753, NA20818, NA10847, HG01353, HG00313, HG00154, NA18951, NA19210, NA12489, HG00282, HG00328, NA19152, HG00732, NA19391, NA19327, HG00556, HG00583, HG00500, NA19788, NA20506, NA18871, NA18976, NA18948, NA18534, NA18981, NA18907, HG01390, HG01047, NA19654, HG01094, HG00324, NA11919, NA20581, NA12829, HG00331, NA11894, NA18912, NA18853, NA18553, NA19099, HG01334, NA19338, NA19761, NA19257, HG00276, NA20828, NA18523, NA19160, NA19395, NA18570, NA18858, NA12043, NA19401, NA19375, NA18533, NA18909, NA11881, HG00336, NA19834, NA18952, NA19147, NA18517, NA18564, HG00580, HG00136, NA20804, NA19380, NA19144, HG01174, HG00116, HG01108, NA19360, HG00256, NA19398, NA19328, NA06994, NA19248, NA18971, NA12749, HG00656, HG00310, NA19102, NA18873, NA20758, NA19116, NA19213, NA18972, HG00343, NA18983, HG00372, HG00472, NA07056, NA19129, NA19755, NA18488, NA19758, NA19316, HG01125, NA18968, HG00345, NA12006, NA07000, NA18622, HG01437, HG01061, HG00437, NA19153, NA18965, NA20772
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668466
Frequency
Sample Size1151
Observed Gain0
Observed Loss209
Observed Complex0
Frequencyn/a


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