A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065620



Internal ID19154839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79061951..79086081hg38UCSC Ensembl
Innerchr16:79095848..79119978hg19UCSC Ensembl
Innerchr16:77653349..77677479hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3824131
hg1924131
hg1824131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559768
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)nsv1065620
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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