A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518005



Internal ID15445298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:67400583..67407433hg38UCSC Ensembl
Innerchr8:68312818..68319668hg19UCSC Ensembl
Innerchr8:68475372..68482222hg18UCSC Ensembl
Innerchr8:68475372..68482222hg17UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg386851
hg196851
hg186851
hg176851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695418
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518005
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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