A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682045



Internal ID15418697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35234530..35545430hg38UCSC Ensembl
Innerchr16:34468901..34779801hg19UCSC Ensembl
Innerchr16:34326402..34637302hg18UCSC Ensembl
Innerchr16:34326402..34637302hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38310901
hg19310901
hg18310901
hg17310901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516385
Supporting Variants
Samples
Known GenesLOC100130700, LOC146481, LOC283914
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682045
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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