A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697749



Internal ID15087715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6392183..6395292hg38UCSC Ensembl
Innerchr16:6442184..6445293hg19UCSC Ensembl
Innerchr16:6382185..6385294hg18UCSC Ensembl
Innerchr16:6382185..6385294hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg383110
hg193110
hg183110
hg173110
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521039
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697749
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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