A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526850



Internal ID15107457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:108287357..108290686hg38UCSC Ensembl
Innerchr13:108939705..108943034hg19UCSC Ensembl
Innerchr13:107737706..107741035hg18UCSC Ensembl
Innerchr13:107737706..107741035hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg383330
hg193330
hg183330
hg173330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703208
Samples
Known GenesTNFSF13B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526850
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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