A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852405



Internal ID15799675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6869983..6914962hg38UCSC Ensembl
Innerchr16:6919984..6964963hg19UCSC Ensembl
Innerchr16:6859985..6904964hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3844980
hg1944980
hg1844980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571377
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)nssv852405
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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