A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690676



Internal ID15427328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80008909..80016373hg38UCSC Ensembl
Innerchr16:80042806..80050270hg19UCSC Ensembl
Innerchr16:78600307..78607771hg18UCSC Ensembl
Innerchr16:78600307..78607771hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg387465
hg197465
hg187465
hg177465
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520894
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690676
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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