A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006482



Internal ID20573522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108282240..108282713hg38UCSC Ensembl
chr13:108934588..108935061hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491925
Supporting Variants
Samples
Known GenesTNFSF13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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