A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518010



Internal ID15445303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:52787725..52799510hg38UCSC Ensembl
Innerchr16:52821637..52833422hg19UCSC Ensembl
Innerchr16:51379138..51390923hg18UCSC Ensembl
Innerchr16:51379138..51390923hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3811786
hg1911786
hg1811786
hg1711786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695422
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518010
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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