A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519065



Internal ID15099672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9108113..9152590hg38UCSC Ensembl
Innerchr16:9201970..9246447hg19UCSC Ensembl
Innerchr16:9109471..9153948hg18UCSC Ensembl
Innerchr16:9109471..9153948hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3844478
hg1944478
hg1844478
hg1744478
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696537
Samples
Known GenesC16orf72
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519065
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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