A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065743



Internal ID19154962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78851285..78946532hg38UCSC Ensembl
Innerchr16:78885182..78980429hg19UCSC Ensembl
Innerchr16:77442683..77537930hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3895248
hg1995248
hg1895248
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559757
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)nsv1065743
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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