A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696638



Internal ID15086604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6286736..6475982hg38UCSC Ensembl
Innerchr16:6336737..6525983hg19UCSC Ensembl
Innerchr16:6276738..6465984hg18UCSC Ensembl
Innerchr16:6276738..6465984hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38189247
hg19189247
hg18189247
hg17189247
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519158
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696638
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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