A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618226



Internal ID6658421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102558699..102560292hg38UCSC Ensembl
Innerchr8:102558700..102560292hg38UCSC Ensembl
Outerchr8:102558699..102560293hg38UCSC Ensembl
chr8:103570927..103572520hg19UCSC Ensembl
Innerchr8:103570928..103572520hg19UCSC Ensembl
Outerchr8:103570927..103572521hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381594
hg191594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13270854, essv13270928, essv13270858, essv13270914, essv13270849, essv13270856, essv13270881, essv13270866, essv13270879, essv13270908, essv13270862, essv13270904, essv13270859, essv13270871, essv13270929, essv13270870, essv13270852, essv13270921, essv13270889, essv13270913, essv13270925, essv13270903, essv13270894, essv13270924, essv13270869, essv13270850, essv13270868, essv13270891, essv13270915, essv13270886, essv13270887, essv13270877, essv13270851, essv13270857, essv13270927, essv13270901, essv13270876, essv13270867, essv13270900, essv13270898, essv13270893, essv13270909, essv13270864, essv13270918, essv13270847, essv13270916, essv13270917, essv13270855, essv13270897, essv13270911, essv13270906, essv13270875, essv13270860, essv13270923, essv13270884, essv13270888, essv13270922, essv13270895, essv13270863, essv13270865, essv13270885, essv13270890, essv13270907, essv13270873, essv13270883, essv13270899, essv13270853, essv13270848, essv13270896, essv13270874, essv13270878, essv13270880, essv13270861, essv13270905, essv13270920, essv13270910, essv13270882, essv13270892, essv13270926, essv13270919, essv13270912, essv13270872, essv13270902
SamplesHG01986, HG02890, HG01412, NA19397, HG02481, HG01303, NA19909, HG03548, NA18861, NA19378, HG03517, HG03247, NA18917, HG02891, HG02012, HG01305, NA18878, HG03172, HG03095, HG03133, NA19319, NA18489, NA19119, NA19457, HG02505, NA19922, HG03189, NA18874, HG03268, NA18868, HG02461, NA19471, HG03114, HG02715, HG03343, HG02570, HG03061, NA19403, HG03088, NA19347, NA19043, HG02307, HG01077, HG01880, HG03124, HG03294, HG03472, HG03476, HG02817, HG02577, HG02445, HG03397, NA18856, HG01182, HG02881, NA19320, HG03024, HG03046, HG02585, HG02332, NA20296, HG02813, NA19017, NA19375, NA19440, NA19309, NA19149, HG03367, NA19712, HG00734, HG02814, HG03108, NA19376, HG03157, HG03049, HG02053, HG03258, HG02768, HG03538, HG03401, NA19430, NA18505, NA19463
Known GenesODF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618226
Frequency
Sample Size2504
Observed Gain0
Observed Loss83
Observed Complex0
Frequencyn/a


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