A curated catalogue of human genomic structural variation

Variant Details

Variant: dgv658e214

Internal ID20122081
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27755925..27983639hg38UCSC Ensembl
chr19:28246833..28474547hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3644081, esv3644080
SamplesHG01878, HG02122, HG02724, HG02725, HG03697, HG03755, HG03968, HG04225, HG03858, HG02657, HG03705, HG03900, HG03760, HG03861, HG02275, HG03668, HG02736, HG03729, HG03784, HG01852, HG03479, HG01089, HG03744, HG00705, HG02661, HG03711, HG01859, HG03478, HG03856, HG03868, HG02727, HG02549, HG01970, HG02601, HG02792, HG04096, HG01777, HG01845, HG02450, HG02648, HG01197, HG03896, HG04056, HG01325, HG01850, HG02783, HG02681, HG04229, HG03642, HG03653, HG02010, HG03746, HG02660, HG01920, HG01844, HG03491, HG03951, HG03967, HG04002, HG04214, HG04200, HG03696, HG04094, HG04020, HG03714, HG02150, HG03949, HG01968, HG04106, HG04209, HG03863, HG03897, HG03752, HG03836, HG03652, HG01917, HG02775, HG04206, HG01092, HG02699, HG04075, NA19735, HG01312, HG01392, HG02700, HG03779, HG03882, NA19917, HG03953, HG01402, HG03686, NA19722, HG01061, HG02577, HG03867, HG03899, HG01395, HG01851, HG02658, HG03717, HG03681, HG04198, HG03770, HG03787, HG03862, HG02557, HG03844, HG03805, HG01396, HG03965, HG03851, HG03871, HG01977, HG02348, HG02078, HG01161, HG04222, HG04063, HG03864, NA19663, HG01187, HG03781, HG04227, HG01599, HG03971, HG03685, HG03722, HG03848, HG02737, HG03742, HG02076, HG03780, HG03895, HG02058, HG02603, HG03869, HG00742, HG01874, HG01974, HG03731, HG03757, HG03773, HG02304, HG03786, HG04017, HG01600, HG02490, HG02127, HG04025, HG01413, HG03998, HG03792, HG02102, HG02541, HG03995, HG00732, HG03660, HG03753, HG03743, HG03649, HG04070, HG02786, HG03754, HG02073, HG03782, HG02439, HG01853, HG03944, HG04080, HG04239, HG01967, HG03849, HG01170, HG02558, HG03619, HG03974, HG01176, HG02069, HG03740, HG03873, HG02787, HG01889, HG02651, HG02494, HG02780, HG03778, HG03788, HG03733, HG04212, HG03645, HG02545, HG04093, HG01060, HG02072, HG02536, HG03738, HG03978, HG03228, HG03713, HG03945, HG01077, HG02690, HG03943, HG01921, HG01991, HG02881, HG02345, HG04235, HG01063, HG01162, HG02281, HG03691, HG02491, HG03237, HG01095, HG02128, HG04033, HG03875, HG01971, HG01973, HG03772, HG04022, HG03745, HG03789, HG03790, HG03679, HG04047, HG02070, HG01953, HG03866, HG04019, HG01872, HG02688, HG03238, HG03694, HG03986, HG02604, HG03644, HG03771, HG03716, HG02075, NA19741, HG03702, HG01303, HG01893, HG03872, HG03018, HG02262, HG04035, HG02079, HG03999, HG01412, HG02252, HG03708, HG01992, HG04018, HG02687, HG03890, HG04039, HG01886, HG01323, HG03857, HG01855, HG03640, HG03718, HG02682, HG03016, HG03838, HG02728, HG04015, HG02555, HG04006, HG03695, HG03837, HG02784, HG03720, HG01857, HG01890, HG02493, HG03730, HG01976, HG03490, HG03991, HG02774, HG01980, HG03777, HG03775, HG02253, HG04107, HG03689, HG01870, HG03625, HG02691, HG02580, HG03684, HG02057, HG02477, HG03963, HG02793, HG01241, HG01846, HG03785, HG01302, HG04003, HG01072, NA20785, HG02697, HG01075, HG03977, HG01918, HG04202, HG01873, HG02546, HG03703, HG02655, HG02600, HG03874, HG01858, HG03693, HG03634, HG01849, HG02734, HG04014, HG04211, HG03643, HG01847, HG02014, HG03663, HG03709, HG04026, HG03894, HG02733, HG02652, HG03973, HG01954, HG03680, HG04216, HG01204, HG02790, HG01461, HG01961, HG03960, HG02049, HG04100, HG02789, HG01848, HG01871, HG02778, HG03488, HG03947, HG01841, HG01843, HG03687, HG03756, HG01311, HG03667, HG02455, HG04238, HG04098, HG04210, HG02684, HG03736, HG02654, HG02696, HG01414, HG02009, HG02121
Known GenesLINC00662
PlatformMultiple platforms
Pubmed ID21293372
Accession Number(s)dgv658e214
Sample Size2504
Observed Gain367
Observed Loss0
Observed Complex0

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