A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623104



Internal ID7009961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45679265..45697066hg38UCSC Ensembl
Innerchr10:45679265..45697066hg38UCSC Ensembl
Outerchr10:45678765..45697566hg38UCSC Ensembl
chr10:46174713..46192514hg19UCSC Ensembl
Innerchr10:46174713..46192514hg19UCSC Ensembl
Outerchr10:46174213..46193014hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3817802
hg1917802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13770816, essv13770869, essv13770899, essv13770836, essv13770799, essv13770730, essv13770863, essv13770896, essv13770804, essv13770834, essv13770812, essv13770788, essv13770864, essv13770756, essv13770919, essv13770782, essv13770755, essv13770898, essv13770809, essv13770727, essv13770767, essv13770775, essv13770887, essv13770764, essv13770758, essv13770818, essv13770865, essv13770769, essv13770789, essv13770784, essv13770761, essv13770829, essv13770914, essv13770781, essv13770902, essv13770854, essv13770737, essv13770833, essv13770763, essv13770827, essv13770906, essv13770844, essv13770920, essv13770842, essv13770826, essv13770797, essv13770823, essv13770779, essv13770881, essv13770831, essv13770750, essv13770878, essv13770901, essv13770895, essv13770822, essv13770796, essv13770873, essv13770754, essv13770917, essv13770880, essv13770800, essv13770861, essv13770884, essv13770860, essv13770862, essv13770848, essv13770935, essv13770821, essv13770746, essv13770897, essv13770785, essv13770925, essv13770905, essv13770851, essv13770790, essv13770926, essv13770793, essv13770760, essv13770850, essv13770807, essv13770858, essv13770883, essv13770872, essv13770915, essv13770912, essv13770889, essv13770910, essv13770933, essv13770801, essv13770893, essv13770866, essv13770870, essv13770813, essv13770846, essv13770839, essv13770808, essv13770747, essv13770748, essv13770787, essv13770741, essv13770806, essv13770728, essv13770909, essv13770735, essv13770803, essv13770900, essv13770931, essv13770814, essv13770810, essv13770773, essv13770757, essv13770890, essv13770929, essv13770753, essv13770733, essv13770894, essv13770828, essv13770830, essv13770923, essv13770778, essv13770783, essv13770752, essv13770820, essv13770791, essv13770885, essv13770777, essv13770857, essv13770740, essv13770867, essv13770772, essv13770891, essv13770882, essv13770907, essv13770847, essv13770835, essv13770817, essv13770794, essv13770874, essv13770738, essv13770922, essv13770849, essv13770837, essv13770936, essv13770765, essv13770802, essv13770734, essv13770853, essv13770932, essv13770877, essv13770792, essv13770739, essv13770774, essv13770841, essv13770786, essv13770795, essv13770886, essv13770805, essv13770911, essv13770855, essv13770751, essv13770745, essv13770927, essv13770888, essv13770732, essv13770918, essv13770736, essv13770815, essv13770759, essv13770913, essv13770798, essv13770762, essv13770749, essv13770819, essv13770934, essv13770928, essv13770924, essv13770875, essv13770845, essv13770930, essv13770824, essv13770868, essv13770876, essv13770743, essv13770916, essv13770840, essv13770843, essv13770908, essv13770892, essv13770811, essv13770729, essv13770832, essv13770780, essv13770744, essv13770838, essv13770852, essv13770859, essv13770825, essv13770879, essv13770921, essv13770771, essv13770770, essv13770742, essv13770903, essv13770871, essv13770766, essv13770904, essv13770731, essv13770856, essv13770776, essv13770768
SamplesHG04212, HG00114, NA20339, HG03366, HG01412, NA19058, NA21097, HG03484, HG02652, HG00231, NA18924, HG00102, NA19664, HG01610, HG00351, HG02035, HG01602, HG02337, HG01326, NA11933, HG03449, HG02061, NA20532, HG04002, HG02891, NA18639, HG02476, HG00699, HG01686, HG02058, NA20805, HG03018, HG03515, HG03297, NA20346, HG02536, NA19443, HG01051, NA19314, NA18633, NA18962, NA12155, NA18627, HG03095, HG02792, NA19068, NA18563, HG03082, HG03770, NA19315, HG01779, NA20589, HG01064, HG00674, NA20317, NA12348, HG01710, HG01599, NA19131, NA18618, NA19062, HG03105, NA19023, NA19771, NA12287, HG03479, HG02816, HG02603, HG03079, HG01859, HG00158, NA19404, NA19041, HG01067, HG00335, HG02067, HG02573, HG02224, NA18977, HG03212, HG02187, NA19372, NA19172, NA19471, HG00406, NA18990, HG01121, NA19209, HG02623, NA19456, NA18975, NA20587, NA18973, HG03369, HG00253, NA20755, NA20318, NA19921, NA19027, HG03270, HG03169, HG03697, NA18613, NA18538, HG00176, NA19091, NA19707, HG02793, HG01122, NA19006, HG00557, HG04062, NA20809, NA19086, HG01344, NA20521, NA19984, HG01684, HG02511, HG01515, NA20862, HG03491, HG00533, HG01768, HG03771, HG00500, NA20506, HG02165, HG00551, NA18981, HG01630, HG03294, HG01092, NA20581, HG00331, NA20881, HG02141, NA19001, HG03974, HG02283, HG00157, NA19338, HG02256, HG01890, NA19225, NA12144, NA18523, NA19318, HG04159, HG02586, NA18570, HG02484, NA19035, NA19017, HG01444, HG03598, NA18542, NA19440, NA19309, HG02684, NA18909, NA18952, HG03461, HG02049, HG01878, NA19454, HG00136, NA18941, NA19090, NA20520, NA07051, NA19010, NA12046, NA20362, HG01375, NA19835, NA18629, HG03473, HG00116, NA20516, NA19083, HG02580, HG03103, NA20357, HG02700, NA18971, HG01491, HG03157, NA19472, HG03066, NA19060, HG01055, NA20807, HG00280, HG00343, HG01251, NA19661, HG01377, HG00472, HG03611, NA19312, NA12890, HG02805, HG02351, NA19063, HG01776, HG02060, NA18965, NA11832, HG03196
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623104
Frequency
Sample Size2504
Observed Gain0
Observed Loss210
Observed Complex0
Frequencyn/a


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