A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852366



Internal ID15799636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6568259..6599734hg38UCSC Ensembl
Innerchr16:6618260..6649735hg19UCSC Ensembl
Innerchr16:6558261..6589736hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3831476
hg1931476
hg1831476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571330
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)nssv852366
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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