A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635779



Internal ID7022577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22095526..22146218hg38UCSC Ensembl
chr15:22383477..22434169hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3850693
hg1950693
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv437e214
Supporting Variantsessv15163740, essv15163733, essv15163756, essv15163763, essv15163859, essv15163852, essv15163818, essv15163815, essv15163732, essv15163856, essv15163806, essv15163753, essv15163795, essv15163743, essv15163813, essv15163745, essv15163731, essv15163807, essv15163846, essv15163826, essv15163812, essv15163821, essv15163797, essv15163728, essv15163765, essv15163739, essv15163802, essv15163799, essv15163735, essv15163778, essv15163851, essv15163853, essv15163784, essv15163809, essv15163854, essv15163757, essv15163722, essv15163742, essv15163783, essv15163741, essv15163848, essv15163833, essv15163819, essv15163772, essv15163860, essv15163822, essv15163835, essv15163791, essv15163747, essv15163790, essv15163762, essv15163748, essv15163839, essv15163794, essv15163789, essv15163838, essv15163746, essv15163793, essv15163801, essv15163777, essv15163768, essv15163749, essv15163855, essv15163770, essv15163744, essv15163714, essv15163785, essv15163825, essv15163724, essv15163779, essv15163761, essv15163849, essv15163796, essv15163782, essv15163828, essv15163804, essv15163766, essv15163717, essv15163810, essv15163760, essv15163780, essv15163752, essv15163792, essv15163858, essv15163836, essv15163710, essv15163808, essv15163764, essv15163736, essv15163711, essv15163737, essv15163798, essv15163841, essv15163830, essv15163811, essv15163758, essv15163750, essv15163769, essv15163738, essv15163719, essv15163837, essv15163803, essv15163844, essv15163723, essv15163845, essv15163759, essv15163712, essv15163857, essv15163767, essv15163754, essv15163847, essv15163832, essv15163816, essv15163840, essv15163773, essv15163725, essv15163729, essv15163715, essv15163834, essv15163805, essv15163820, essv15163781, essv15163842, essv15163721, essv15163850, essv15163755, essv15163829, essv15163843, essv15163787, essv15163800, essv15163814, essv15163730, essv15163720, essv15163727, essv15163788, essv15163718, essv15163817, essv15163827, essv15163713, essv15163824, essv15163776, essv15163775, essv15163751, essv15163716, essv15163771, essv15163823, essv15163831, essv15163786, essv15163734, essv15163774, essv15163726
SamplesHG03690, HG02386, HG02339, HG00592, NA20529, HG01054, NA19397, HG03163, NA19399, HG01860, NA20783, HG02702, NA20899, HG03247, NA19704, HG02337, HG02029, HG03241, NA18979, HG00457, NA20802, NA19350, HG01806, NA19092, HG02804, HG02600, HG02624, HG03518, NA20346, NA20507, NA19669, HG03372, HG02023, HG03478, HG00693, HG03199, HG03235, HG00251, HG03168, HG02156, HG03976, HG02155, NA20317, HG01599, NA18942, NA19062, NA18574, HG04182, HG03342, HG02655, HG03234, NA19384, HG00537, HG02111, HG03851, HG00130, HG03887, HG03460, HG02561, HG00683, HG02187, NA20340, NA19024, HG04106, HG01284, NA19901, HG03750, HG03394, NA18973, NA21105, HG04075, NA18638, NA20753, HG00133, HG03343, HG03780, NA20535, NA19210, NA19437, HG00183, HG00282, HG03714, HG02070, HG01595, HG01857, HG02697, HG03760, HG01790, HG00657, HG01879, NA18939, NA19982, HG02307, HG03945, HG00708, NA18907, HG03967, HG03311, HG03085, HG00684, HG01613, NA19001, HG00525, HG00157, HG03953, HG03971, HG02601, HG01865, HG03898, HG02635, HG01896, HG03743, NA21143, NA18632, HG02667, HG00119, HG03367, NA19712, NA18950, NA19037, HG03458, HG03117, HG02923, NA19380, NA19144, HG02982, HG01598, NA20544, NA21094, HG01342, HG01862, HG03703, HG03565, HG00672, HG02379, NA19785, NA19713, HG03060, NA21101, NA19185, HG01872, NA19711, HG03401, NA18983, HG03162, HG02861, HG01378, HG00171, HG01583, HG00362, NA21120
Known GenesOR4N3P, OR4N4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635779
Frequency
Sample Size2504
Observed Gain151
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer