A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520905



Internal ID15101512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6391934..6392183hg38UCSC Ensembl
Innerchr16:6441935..6442184hg19UCSC Ensembl
Innerchr16:6381936..6382185hg18UCSC Ensembl
Innerchr16:6381936..6382185hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38250
hg19250
hg18250
hg17250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693511, nssv681575, nssv677298
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520905
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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