A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852392



Internal ID15799662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6771871..6890632hg38UCSC Ensembl
Innerchr16:6821872..6940633hg19UCSC Ensembl
Innerchr16:6761873..6880634hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38118762
hg19118762
hg18118762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571362
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852392
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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