A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518503



Internal ID15445796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55468464..55470609hg38UCSC Ensembl
Innerchr16:55502376..55504521hg19UCSC Ensembl
Innerchr16:54059877..54062022hg18UCSC Ensembl
Innerchr16:54059877..54062022hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg382146
hg192146
hg182146
hg172146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695944
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518503
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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