A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv236e214



Internal ID20121659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132053654..132060279hg38UCSC Ensembl
chr11:131923548..131930173hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg386626
hg196626
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
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv236e214
Frequency
Sample Size2504
Observed Gain390
Observed Loss0
Observed Complex0
Frequencyn/a


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