A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040937



Internal ID18783468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8938995..9233787hg38UCSC Ensembl
Innerchr16:9032852..9327644hg19UCSC Ensembl
Innerchr16:8940353..9235145hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38294793
hg19294793
hg18294793
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718871
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)nsv1040937
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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