A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852371



Internal ID15799641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6607850..6627776hg38UCSC Ensembl
Innerchr16:6657851..6677777hg19UCSC Ensembl
Innerchr16:6597852..6617778hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3819927
hg1919927
hg1819927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571340
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)nssv852371
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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