A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622195



Internal ID7009054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4395503..4399198hg38UCSC Ensembl
Innerchr10:4395504..4399198hg38UCSC Ensembl
Outerchr10:4395503..4399199hg38UCSC Ensembl
chr10:4437695..4441390hg19UCSC Ensembl
Innerchr10:4437696..4441390hg19UCSC Ensembl
Outerchr10:4437695..4441391hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383696
hg193696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13682817, essv13682809, essv13682837, essv13682889, essv13682902, essv13682900, essv13682879, essv13682848, essv13682884, essv13682805, essv13682811, essv13682842, essv13682905, essv13682887, essv13682914, essv13682860, essv13682895, essv13682845, essv13682908, essv13682896, essv13682812, essv13682868, essv13682833, essv13682904, essv13682916, essv13682898, essv13682899, essv13682828, essv13682877, essv13682897, essv13682874, essv13682827, essv13682836, essv13682870, essv13682839, essv13682834, essv13682913, essv13682850, essv13682892, essv13682849, essv13682822, essv13682885, essv13682873, essv13682854, essv13682891, essv13682853, essv13682814, essv13682901, essv13682859, essv13682818, essv13682881, essv13682865, essv13682893, essv13682858, essv13682852, essv13682871, essv13682816, essv13682863, essv13682869, essv13682813, essv13682826, essv13682806, essv13682830, essv13682831, essv13682843, essv13682918, essv13682803, essv13682920, essv13682829, essv13682872, essv13682864, essv13682808, essv13682919, essv13682856, essv13682894, essv13682841, essv13682862, essv13682912, essv13682819, essv13682851, essv13682875, essv13682802, essv13682810, essv13682888, essv13682847, essv13682861, essv13682906, essv13682825, essv13682846, essv13682890, essv13682882, essv13682820, essv13682855, essv13682903, essv13682907, essv13682815, essv13682804, essv13682917, essv13682880, essv13682832, essv13682840, essv13682867, essv13682807, essv13682857, essv13682883, essv13682821, essv13682886, essv13682866, essv13682823, essv13682824, essv13682878, essv13682909, essv13682876, essv13682844, essv13682835, essv13682838, essv13682911, essv13682915, essv13682910
SamplesHG02339, NA19700, HG01462, NA19399, HG02702, HG03247, HG03300, HG02852, HG02419, NA19350, HG03130, NA19092, NA19819, HG02624, NA19377, HG02536, NA19107, HG03095, NA19171, HG02811, HG03385, NA19307, NA19198, NA20317, HG02756, HG02645, HG03105, NA19904, HG02981, HG02281, NA19404, NA19041, HG03556, HG02315, NA19917, NA19024, NA19235, HG03195, HG02642, NA19385, NA19471, HG03352, NA19026, HG02571, NA19901, NA19189, NA18520, HG02545, HG03583, NA18908, HG02715, HG03369, NA20318, HG03048, NA19908, NA19437, NA18934, HG02334, NA19347, NA19184, HG02511, NA19913, HG01989, NA20126, NA18910, HG01889, NA19118, HG01241, HG03571, NA19338, NA19225, NA18523, HG02332, HG01896, HG02813, NA19440, NA19309, NA19390, NA18909, HG03367, HG02983, NA19435, HG02314, HG03304, HG02558, NA19475, NA19323, NA19117, HG03039, NA20348, NA19248, HG02970, NA19472, HG03313, HG03279, HG03060, HG03351, HG02676, NA19102, HG02679, HG02013, NA19711, HG03077, HG01468, NA19900, HG02052, HG02051, HG03445, HG02861, HG01464, NA18505, NA19129, NA18488, NA19316, NA19312, HG03376, HG01886, HG03303, NA19431
Known GenesLINC00703
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622195
Frequency
Sample Size2504
Observed Gain0
Observed Loss119
Observed Complex0
Frequencyn/a


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