A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696313



Internal ID15086279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7120958..7122067hg38UCSC Ensembl
Innerchr16:7170959..7172068hg19UCSC Ensembl
Innerchr16:7110960..7112069hg18UCSC Ensembl
Innerchr16:7110960..7112069hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381110
hg191110
hg181110
hg171110
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518859
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696313
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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