A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563024



Internal ID16003747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:108285905..108298237hg38UCSC Ensembl
Innerchr13:108938253..108950585hg19UCSC Ensembl
Innerchr13:107736254..107748586hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3812333
hg1912333
hg1812333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3378n54
Supporting Variantsnssv819260
Samples
Known GenesTNFSF13B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563024
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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