A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694877



Internal ID15084843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6622410..6622740hg38UCSC Ensembl
Innerchr16:6672411..6672741hg19UCSC Ensembl
Innerchr16:6612412..6612742hg18UCSC Ensembl
Innerchr16:6612412..6612742hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38331
hg19331
hg18331
hg17331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522105
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694877
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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