A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571359



Internal ID16012082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6746865..6990984hg38UCSC Ensembl
Innerchr16:6796866..7040985hg19UCSC Ensembl
Innerchr16:6736867..6980986hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38244120
hg19244120
hg18244120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4893n54
Supporting Variantsnssv852389
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571359
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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