A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676419



Internal ID15066385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80921496..80955962hg38UCSC Ensembl
Innerchr16:80955393..80989859hg19UCSC Ensembl
Innerchr16:79512894..79547360hg18UCSC Ensembl
Innerchr16:79512894..79547360hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3834467
hg1934467
hg1834467
hg1734467
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520122
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676419
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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