A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666117



Internal ID9932222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133111230..133111738hg38UCSC Ensembl
Outerchr10:133111177..133111793hg38UCSC Ensembl
Innerchr10:134924734..134925242hg19UCSC Ensembl
Outerchr10:134924681..134925297hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv179e199
Supporting Variantsessv6537817, essv5754305, essv6328938, essv6159778, essv5827322, essv6514160, essv6515751, essv6516330, essv5751272, essv6200785, essv5920167, essv5439470, essv5421154, essv5929921, essv5465236, essv5454797, essv6088662, essv6326262, essv5910231, essv5488994, essv6229372, essv5883244, essv5781583, essv6376045, essv5466408, essv5859748, essv6337967, essv5936964, essv5459762, essv5424616, essv6590614, essv6130009, essv5716092, essv5584784, essv6003136, essv6471780, essv6117029, essv6496953, essv5576468, essv5533538, essv6151883, essv5821016, essv5634714, essv5438104, essv5905571, essv5752108, essv6553267, essv6558997, essv6281971, essv6067568, essv6009695, essv5709905, essv6125614, essv6117966, essv5800981, essv6234214, essv5759931, essv6438469, essv6133121, essv5545835, essv6249350, essv5649093, essv5431351, essv6236872, essv6305442, essv6131096, essv6251235, essv6273653, essv5453902, essv6032799, essv6527371, essv6056878, essv5429926, essv6447832, essv5713209, essv6497373, essv6324009, essv5445431, essv5582334, essv5817926, essv6164979, essv5863719, essv5509446, essv5479753, essv6439468, essv5522039, essv6462688, essv6460989, essv5751145, essv5692052, essv5774659, essv5402402, essv6273234, essv5633893, essv6280674, essv5675011, essv6143184, essv6077366, essv5874719, essv5679296, essv6192166, essv5563068, essv6546860, essv6006557, essv5514918, essv6493302, essv5516168, essv5405247, essv5785609, essv6356199, essv6326237, essv6005889, essv5926215, essv5425549, essv6439687, essv6445659, essv5797999, essv6097265, essv6145628, essv6000336, essv5450910, essv5886159, essv5899057, essv5833883, essv5651517, essv6297273, essv6296385, essv5847940, essv5934001, essv5469618, essv5408463, essv5848379, essv6167804, essv5811102, essv6022149, essv5533973, essv6559299, essv6455106, essv6138544, essv6125976, essv5416036, essv6337149, essv6218976, essv6106263, essv5865026, essv6344100, essv5918136, essv5561343, essv6324290, essv6562649, essv5924877, essv6550267, essv5536690, essv5815283, essv6383262, essv6203341, essv6084722, essv5787614, essv5642964, essv5729217, essv6486593, essv6407013, essv6283782, essv5888980, essv5928377, essv5733527, essv5702575, essv5543456, essv5445163, essv5409333, essv5402234, essv5970839, essv6583807, essv6487041, essv6329004, essv6019680, essv6367565, essv6308314, essv5553088, essv5448834, essv6407179, essv5942806, essv6257763, essv6493203, essv6209849, essv6128598, essv6540823, essv5830241, essv5593287, essv6425067, essv6034414, essv6093950, essv6039706, essv5428988, essv6556431, essv6478486, essv6071695, essv5493510, essv6342609, essv5475989, essv6151956, essv6394290, essv5809217, essv6453863, essv6085672, essv6273055, essv5627742, essv5600479, essv6436548, essv6255486, essv6473114, essv6078960, essv5507059, essv6083475, essv6089917, essv6077284, essv5657470, essv6134442, essv5496736, essv6173426, essv5614210, essv6595649, essv6532169, essv6382862, essv5611947, essv5963720, essv5913764
SamplesHG00626, HG01060, NA19701, HG00650, NA19700, NA19703, NA19055, NA19397, HG00608, NA19909, HG00142, HG01359, HG00524, NA19399, HG01052, NA18980, NA11920, HG01188, NA18599, HG01389, HG01374, HG00318, NA19359, NA18486, HG00699, NA18545, NA19819, NA18596, NA19377, NA18530, NA12058, NA18606, NA18616, HG01461, HG00654, NA19443, NA19190, NA18633, NA18602, NA18627, HG00271, HG00663, NA19746, NA19396, HG00138, NA19076, HG00501, NA18597, HG01351, NA19448, NA18595, HG01488, HG00702, HG00689, HG00448, HG00173, NA18635, NA19198, NA12348, HG00634, NA18960, HG01354, NA19313, NA19088, HG00247, HG00369, HG00334, NA19681, HG00311, NA19130, NA19079, HG00590, NA18611, NA19404, HG01134, HG00512, HG00281, HG00277, HG01069, NA19383, HG00106, NA20775, HG01170, HG00236, NA18977, NA19719, NA19372, NA18560, HG00534, NA19075, HG00422, NA19471, HG00309, HG00427, HG00160, NA18990, HG00159, HG01048, NA19445, HG00326, HG00530, HG00419, HG00464, NA18614, HG01353, HG00543, HG00313, HG01183, HG01136, HG00154, HG00149, NA18544, NA18605, NA18613, HG00731, HG00629, NA19657, HG00443, NA18538, HG00183, HG00282, NA19056, HG00596, HG00557, HG00328, HG00428, HG00732, HG00653, HG00701, HG00657, NA20760, NA19717, NA19455, NA19663, HG00584, HG00533, HG00583, NA18637, HG00500, NA18910, HG00619, HG00708, HG01047, NA18573, NA19774, NA19084, HG00531, HG00479, NA12829, HG00331, HG00684, HG01101, HG00613, HG00140, NA19009, NA18555, NA19452, HG00463, HG00126, NA19625, HG01107, NA19436, NA18546, NA18953, NA19401, NA19003, HG00124, NA20773, NA18542, HG00285, NA19834, NA18961, NA18543, NA18559, HG00625, NA18628, NA18950, HG00638, HG00278, NA19380, HG01357, HG00607, NA19439, NA19786, NA19467, NA19083, HG01108, NA19360, HG00256, HG00662, HG00418, NA18615, NA18610, HG01342, HG00620, HG00125, NA19818, HG00672, HG00614, HG00111, HG00578, NA19785, HG01491, NA19223, HG00421, HG00656, HG00342, NA19468, HG01055, HG00123, NA18636, HG00698, NA19116, NA19213, HG01251, HG00377, NA18984, HG01082, NA19463, NA12154, NA18549, HG00180, NA19429, NA19074, HG00437, NA18562, HG00581
Known GenesGPR123
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666117
Frequency
Sample Size1151
Observed Gain0
Observed Loss227
Observed Complex0
Frequencyn/a


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