A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697590



Internal ID15087556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83956484..83966533hg38UCSC Ensembl
Innerchr16:83990089..84000138hg19UCSC Ensembl
Innerchr16:82547590..82557639hg18UCSC Ensembl
Innerchr16:82547590..82557639hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3810050
hg1910050
hg1810050
hg1710050
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517566
Supporting Variants
Samples
Known GenesOSGIN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697590
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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