A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520812



Internal ID15448105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:52005291..52023977hg38UCSC Ensembl
Innerchr16:52039203..52057889hg19UCSC Ensembl
Innerchr16:50596704..50615390hg18UCSC Ensembl
Innerchr16:50596704..50615390hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3818687
hg1918687
hg1818687
hg1718687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694402
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520812
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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