A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067314



Internal ID19156533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78831480..78848543hg38UCSC Ensembl
Innerchr16:78865377..78882440hg19UCSC Ensembl
Innerchr16:77422878..77439941hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3817064
hg1917064
hg1817064
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3038n100
Supporting Variantsnssv3559756
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)nsv1067314
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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