A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609993



Internal ID6996912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93830236..93835368hg38UCSC Ensembl
Innerchr6:93830236..93835368hg38UCSC Ensembl
Outerchr6:93829924..93835697hg38UCSC Ensembl
chr6:94539954..94545086hg19UCSC Ensembl
Innerchr6:94539954..94545086hg19UCSC Ensembl
Outerchr6:94539642..94545415hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg385133
hg195133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12465875, essv12465868, essv12465828, essv12465829, essv12465846, essv12465862, essv12465889, essv12465825, essv12465850, essv12465865, essv12465836, essv12465851, essv12465872, essv12465837, essv12465884, essv12465892, essv12465887, essv12465863, essv12465864, essv12465869, essv12465844, essv12465885, essv12465856, essv12465866, essv12465874, essv12465854, essv12465871, essv12465870, essv12465833, essv12465876, essv12465853, essv12465882, essv12465861, essv12465831, essv12465826, essv12465848, essv12465886, essv12465855, essv12465838, essv12465839, essv12465832, essv12465878, essv12465830, essv12465840, essv12465880, essv12465879, essv12465849, essv12465894, essv12465845, essv12465824, essv12465859, essv12465857, essv12465877, essv12465888, essv12465883, essv12465834, essv12465847, essv12465891, essv12465827, essv12465841, essv12465842, essv12465852, essv12465860, essv12465823, essv12465873, essv12465867, essv12465890, essv12465893, essv12465881, essv12465835, essv12465843, essv12465858
SamplesHG03514, HG03096, HG02496, NA18924, NA19466, HG01885, NA19399, HG02973, HG03175, NA18917, HG03130, NA18504, NA19098, HG02769, NA18988, NA19107, NA19374, NA19379, NA18489, NA19131, NA18916, HG03342, NA19904, HG03520, HG03189, HG03268, HG03045, HG02588, HG02545, HG02716, HG02442, HG02977, NA19210, HG03132, HG03363, HG01200, NA19462, NA19152, NA19984, HG01882, NA19043, HG02322, NA18871, HG03159, HG03311, HG03123, NA19114, NA20299, NA19118, HG02445, HG01241, HG03571, HG03024, HG03046, NA19149, HG03367, NA19019, HG02546, NA18992, HG02839, HG02317, HG02558, NA19475, NA19117, HG02974, NA19030, HG02947, HG02805, HG03129, NA19214, HG03265, HG03196
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609993
Frequency
Sample Size2504
Observed Gain0
Observed Loss72
Observed Complex0
Frequencyn/a


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