A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557112



Internal ID18508707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8894733..9125030hg38UCSC Ensembl
Innerchr16:8988590..9218887hg19UCSC Ensembl
Innerchr16:8896091..9126388hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38230298
hg19230298
hg18230298
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049081
Supporting Variants
Samples
Known GenesC16orf72, USP7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557112
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer