A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017329



Internal ID19106546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2473547..2725657hg38UCSC Ensembl
Innerchr8:2330755..2583198hg19UCSC Ensembl
Innerchr8:2318162..2570605hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38252111
hg19252444
hg18252444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6820n100
Supporting Variantsnssv3675272, nssv3675263, nssv3675273, nssv3675252, nssv3757816, nssv3757814, nssv3675257, nssv3757815, nssv3675262, nssv3675269, nssv3757811, nssv3757812, nssv3675270, nssv3675264, nssv3675254, nssv3675267, nssv3675275, nssv3675271, nssv3675266, nssv3675259, nssv3675260, nssv3675256, nssv3675274, nssv3675261, nssv3675255, nssv3675268, nssv3675258, nssv3757813, nssv3675253, nssv3675265
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017329
Frequency
Sample Size11257
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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