A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695527



Internal ID15085493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8327165..8534663hg38UCSC Ensembl
Innerchr16:8377167..8584665hg19UCSC Ensembl
Innerchr16:8317168..8524666hg18UCSC Ensembl
Innerchr16:8317168..8524666hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38207499
hg19207499
hg18207499
hg17207499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518113
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695527
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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