A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852391



Internal ID15799661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6761162..6967914hg38UCSC Ensembl
Innerchr16:6811163..7017915hg19UCSC Ensembl
Innerchr16:6751164..6957916hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38206753
hg19206753
hg18206753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571361
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)nssv852391
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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