A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697924



Internal ID15087890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7065289..7115349hg38UCSC Ensembl
Innerchr16:7115290..7165350hg19UCSC Ensembl
Innerchr16:7055291..7105351hg18UCSC Ensembl
Innerchr16:7055291..7105351hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3850061
hg1950061
hg1850061
hg1750061
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521317
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697924
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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