A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521703



Internal ID15102310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23074311..23103528hg38UCSC Ensembl
Innerchr16:23085632..23114849hg19UCSC Ensembl
Innerchr16:22993133..23022350hg18UCSC Ensembl
Innerchr16:22993133..23022350hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3829218
hg1929218
hg1829218
hg1729218
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698326
Samples
Known GenesUSP31
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521703
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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