A curated catalogue of human genomic structural variation

Variant Details

Variant: dgv236e214

Internal ID20121659
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132053654..132060279hg38UCSC Ensembl
chr11:131923548..131930173hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3628117, esv3628116
SamplesHG01441, HG01776, NA20903, HG03968, NA20876, NA12154, HG00252, HG01770, HG02250, HG03900, NA18595, HG00182, HG02649, NA18951, NA20527, HG03729, NA20862, HG01353, NA18630, HG00956, NA21110, HG03940, NA20752, HG01089, HG03744, HG03593, NA11920, HG03868, HG00186, HG01105, HG01277, HG01970, HG00160, HG02223, NA20888, NA18545, HG01031, HG01365, HG04090, HG02681, HG04060, NA20800, HG01488, NA12828, NA19795, HG03829, HG01174, NA12005, HG01605, HG00364, HG02375, HG02694, HG04118, NA20805, NA20897, HG00334, HG02277, NA19651, HG00280, HG04214, HG04200, HG03949, HG00253, HG04209, NA19761, HG00353, HG00269, HG03752, HG01597, NA19077, HG02402, HG03941, NA20412, HG01550, HG00158, HG02390, NA11919, HG01384, HG04075, NA20849, HG02700, NA21097, NA20764, HG03882, NA20811, HG02221, HG01061, HG01398, HG01709, HG00692, HG01183, HG03770, HG03787, HG00149, HG02410, HG00338, NA21116, HG02078, NA19075, HG02521, HG04222, NA11995, HG00174, HG03603, HG04063, HG00243, HG00276, HG01187, HG00357, HG04227, HG01747, NA12144, HG03848, NA19684, HG02737, NA19728, HG03780, HG01797, NA12006, HG00306, HG00742, HG01948, HG02151, NA18640, NA18537, NA18747, HG02383, HG01705, HG04025, HG01413, HG04141, HG00360, HG01191, NA18572, NA21128, HG00382, NA06985, HG00629, NA19716, NA20790, HG01766, HG03673, HG04158, NA18986, HG00263, NA12275, NA19005, NA20864, HG01073, NA18558, NA18977, HG03931, NA19901, HG03849, HG00282, HG01170, HG03619, HG01356, NA20814, HG01676, NA11892, NA18564, HG00277, HG03778, HG03800, HG00740, HG00101, HG03733, HG03645, NA21093, HG00341, HG01447, HG00458, NA18562, HG01702, HG04134, NA18974, NA19789, HG01512, HG02690, HG00589, NA20891, HG00674, HG02374, HG00120, NA20858, NA11832, NA12890, NA18999, HG00590, HG01326, HG04155, HG01393, HG02235, HG03772, HG04022, HG00611, HG01334, HG03679, HG02070, NA12413, NA19764, HG02134, HG02688, NA12812, NA20850, HG03644, NA20867, HG02075, HG02230, HG01862, NA18989, NA19719, HG00378, HG00311, HG03815, HG03999, NA18614, NA21086, NA19740, HG02687, NA20846, HG01804, NA21117, HG00238, NA12546, NA20886, HG00142, HG01947, HG02409, HG02476, HG01808, NA20872, HG00623, HG01119, NA11932, HG01177, NA20768, HG01498, HG01791, HG00275, HG00690, HG01842, HG01892, HG03850, NA12717, HG00288, HG03802, HG01522, HG00598, NA20524, NA20804, HG00684, HG02391, NA06994, NA20870, HG01678, HG01781, NA19758, HG00336, HG00476, HG00622, HG01857, HG03826, HG01789, HG02064, NA18555, HG00278, HG03490, HG03991, HG00107, HG02215, HG02425, HG02774, HG03824, NA19746, HG01536, HG03006, HG03689, HG01864, HG02691, HG03684, HG04131, HG01513, NA20887, HG00881, HG01459, HG01518, HG01768, HG01775, HG03698, HG04146, HG00356, HG02793, HG01790, HG01798, NA20514, HG00304, HG02165, NA20522, HG02138, NA20503, HG03985, NA20785, HG02025, NA18952, HG01342, HG02407, HG00731, HG00879, HG00736, HG00384, HG01935, HG04014, NA18639, NA18993, NA19670, HG03611, NA18648, NA11931, HG01085, HG02048, NA20808, HG01528, HG03894, HG01685, HG00375, NA18608, NA20786, HG03234, HG00553, NA21098, HG01131, HG01771, NA20900, HG02231, HG03585, HG01204, NA12776, HG03019, NA20314, HG00557, HG02232, NA20895, HG00146, HG03928, HG01871, HG01551, NA19654, HG01784, HG02003, NA19762, HG00154, HG00321, HG04219, HG04098, NA19067, NA20585, HG04210, NA21137, HG01510, HG03672, HG01796, HG02696, NA19652, HG00583, HG01618, HG03021, NA11994, HG00140, NA18563, NA07357, NA20504, HG01595, NA18644, NA19722, HG03899, HG00231, NA20783, NA20807, HG00141, HG03727, NA11933, NA19774, HG02356, HG03917, NA19658, HG00637, HG00254, NA19663
Known GenesNTM
PlatformMultiple platforms
Pubmed ID21293372
Accession Number(s)dgv236e214
Sample Size2504
Observed Gain390
Observed Loss0
Observed Complex0

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