A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620509



Internal ID7007380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43005069..43033698hg38UCSC Ensembl
chr9:66284867..66313496hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3828630
hg1928630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13493794, essv13493849, essv13493799, essv13493893, essv13493816, essv13493875, essv13493819, essv13493846, essv13493863, essv13493798, essv13493881, essv13493834, essv13493894, essv13493802, essv13493820, essv13493813, essv13493866, essv13493800, essv13493854, essv13493790, essv13493788, essv13493864, essv13493822, essv13493808, essv13493801, essv13493792, essv13493887, essv13493818, essv13493867, essv13493852, essv13493877, essv13493873, essv13493785, essv13493811, essv13493831, essv13493859, essv13493836, essv13493837, essv13493827, essv13493810, essv13493821, essv13493826, essv13493782, essv13493855, essv13493797, essv13493853, essv13493844, essv13493817, essv13493885, essv13493815, essv13493787, essv13493865, essv13493876, essv13493805, essv13493872, essv13493868, essv13493830, essv13493871, essv13493848, essv13493825, essv13493869, essv13493806, essv13493879, essv13493795, essv13493780, essv13493843, essv13493840, essv13493861, essv13493841, essv13493786, essv13493850, essv13493804, essv13493793, essv13493890, essv13493862, essv13493789, essv13493833, essv13493828, essv13493851, essv13493829, essv13493889, essv13493807, essv13493814, essv13493892, essv13493882, essv13493883, essv13493857, essv13493880, essv13493860, essv13493891, essv13493779, essv13493870, essv13493796, essv13493886, essv13493845, essv13493783, essv13493839, essv13493803, essv13493823, essv13493878, essv13493884, essv13493856, essv13493858, essv13493832, essv13493838, essv13493781, essv13493812, essv13493842, essv13493784, essv13493874, essv13493835, essv13493824, essv13493809, essv13493888, essv13493791, essv13493847
SamplesHG02574, NA19222, HG01054, HG03121, NA19204, NA19914, HG03175, HG03517, NA19704, NA18507, HG01389, HG00640, HG02870, HG02323, HG03298, NA12058, HG03515, HG03577, HG03172, HG03372, NA19920, NA18510, NA19107, HG00641, HG03436, HG03086, NA19319, HG03168, HG02810, HG01064, HG02645, HG03105, HG03578, HG03224, HG03040, NA19384, NA19922, HG02562, NA19041, HG01398, HG01495, NA19385, NA19317, HG02588, NA19159, HG03380, NA19239, HG02545, NA20127, NA19451, HG03048, HG02479, HG01603, HG03511, HG03547, NA19184, HG02449, HG01879, HG02554, NA19982, HG03575, NA18910, NA18871, HG02976, HG02537, HG01889, HG03311, HG03563, HG03085, HG02429, HG03476, HG02817, HG02445, NA18499, HG03391, HG01890, NA19095, HG01896, HG03064, NA19206, NA19309, HG02807, NA18909, NA18517, HG02759, HG02546, NA19473, HG02721, HG01551, HG03117, NA20362, NA19835, HG02982, NA19324, HG03304, HG03473, HG03103, HG02771, NA18501, NA20348, HG02971, HG02970, HG01912, HG03258, NA19900, NA19121, HG02947, HG01111, HG03072, NA18511, NA18522, HG02629, HG03439, NA18622, NA19431, HG03196
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620509
Frequency
Sample Size2504
Observed Gain0
Observed Loss116
Observed Complex0
Frequencyn/a


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