A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666944



Internal ID15403596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1261332..1287716hg38UCSC Ensembl
Innerchr16:1311333..1337717hg19UCSC Ensembl
Innerchr16:1251334..1277718hg18UCSC Ensembl
Innerchr16:1251334..1277718hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3826385
hg1926385
hg1826385
hg1726385
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515770
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666944
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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