A curated catalogue of human genomic structural variation

Variant Details

Variant: esv3596953

Internal ID6637223
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89344940..89369511hg38UCSC Ensembl
chr3:89394090..89418661hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11068825, essv11068813, essv11068786, essv11068792, essv11068807, essv11068806, essv11068859, essv11068853, essv11068787, essv11068784, essv11068781, essv11068835, essv11068860, essv11068769, essv11068800, essv11068829, essv11068849, essv11068870, essv11068865, essv11068840, essv11068791, essv11068816, essv11068765, essv11068802, essv11068821, essv11068764, essv11068774, essv11068852, essv11068850, essv11068874, essv11068831, essv11068817, essv11068828, essv11068837, essv11068868, essv11068809, essv11068836, essv11068855, essv11068830, essv11068766, essv11068777, essv11068861, essv11068782, essv11068796, essv11068772, essv11068826, essv11068763, essv11068824, essv11068841, essv11068795, essv11068814, essv11068788, essv11068803, essv11068822, essv11068843, essv11068780, essv11068844, essv11068799, essv11068770, essv11068771, essv11068818, essv11068785, essv11068775, essv11068863, essv11068851, essv11068839, essv11068810, essv11068867, essv11068873, essv11068846, essv11068793, essv11068857, essv11068797, essv11068866, essv11068827, essv11068838, essv11068869, essv11068872, essv11068805, essv11068862, essv11068832, essv11068871, essv11068790, essv11068819, essv11068833, essv11068794, essv11068783, essv11068845, essv11068858, essv11068773, essv11068778, essv11068789, essv11068842, essv11068834, essv11068804, essv11068798, essv11068820, essv11068864, essv11068808, essv11068779, essv11068815, essv11068767, essv11068776, essv11068811, essv11068848, essv11068847, essv11068801, essv11068856, essv11068854, essv11068768, essv11068823, essv11068812
SamplesHG01613, HG03755, HG01515, HG00313, HG01768, NA20514, HG03785, HG01675, HG02371, HG01530, NA20527, HG01612, NA18630, HG01052, NA11920, HG00245, HG00632, HG01800, HG01935, HG01389, NA20775, HG01403, NA20511, HG01085, HG01492, NA20800, HG01685, HG00368, NA20778, HG01350, HG01704, HG01131, HG02231, HG01204, NA19648, HG00366, HG03960, HG04020, HG00253, HG01860, NA20755, HG01682, HG00353, HG03687, HG01521, HG01784, HG00342, HG00266, HG01765, NA20849, HG01510, HG01312, HG01672, HG02700, HG01414, NA18536, HG00140, HG02221, HG01866, HG01785, HG01620, NA12761, NA11843, HG01527, NA11894, NA19679, HG01362, HG01747, HG01874, HG04017, HG01097, HG01280, HG04070, HG04173, HG03931, HG00273, HG01786, NA20774, HG01351, HG01702, HG01880, HG01190, HG04155, HG03589, HG00181, NA20827, HG01673, HG03238, NA20318, HG00311, HG01669, NA19818, HG01390, NA20317, NA20810, HG01164, NA20758, HG02682, NA11932, NA20904, NA20528, HG01522, HG01102, HG02188, HG00336, NA19007, NA19661, NA19779, HG01474, NA19746, HG01067, HG01536
Known GenesEPHA3
PlatformMultiple platforms
Pubmed ID21293372
Accession Number(s)esv3596953
Sample Size2504
Observed Gain0
Observed Loss112
Observed Complex0

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