A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150503



Internal ID15532126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6788397..6877241hg38UCSC Ensembl
Innerchr16:6838398..6927242hg19UCSC Ensembl
Innerchr16:6778399..6867243hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3888845
hg1988845
hg1888845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571363
Supporting Variants
SamplesHGDP01262
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150503
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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