A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685839



Internal ID15422491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63253645..63362102hg38UCSC Ensembl
Innerchr16:63287549..63396006hg19UCSC Ensembl
Innerchr16:61845050..61953507hg18UCSC Ensembl
Innerchr16:61845050..61953507hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38108458
hg19108458
hg18108458
hg17108458
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521142
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685839
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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