A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520619



Internal ID15447912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:145479779..145486771hg38UCSC Ensembl
Innerchr6:145800915..145807907hg19UCSC Ensembl
Innerchr6:145842608..145849600hg18UCSC Ensembl
Innerchr6:145842608..145849600hg17UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg386993
hg196993
hg186993
hg176993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678826, nssv695804, nssv675971, nssv673285
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520619
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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