A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652382



Internal ID15042348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83921780..84002720hg38UCSC Ensembl
Innerchr16:83955385..84036325hg19UCSC Ensembl
Innerchr16:82512886..82593826hg18UCSC Ensembl
Innerchr16:82512886..82593826hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3880941
hg1980941
hg1880941
hg1780941
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517566
Supporting Variants
Samples
Known GenesNECAB2, OSGIN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652382
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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