A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065496



Internal ID19154715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78976130..79022511hg38UCSC Ensembl
Innerchr16:79010027..79056408hg19UCSC Ensembl
Innerchr16:77567528..77613909hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3846382
hg1946382
hg1846382
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559765
Samples
Known GenesWWOX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065496
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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