A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700391



Internal ID15090357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7410809..7411522hg38UCSC Ensembl
Innerchr16:7460810..7461523hg19UCSC Ensembl
Innerchr16:7400811..7401524hg18UCSC Ensembl
Innerchr16:7400811..7401524hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38714
hg19714
hg18714
hg17714
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520018
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700391
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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