A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182001



Internal ID20749041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42554701..42579500hg38UCSC Ensembl
chr13:43128837..43153636hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3824800
hg1924800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481180
Supporting Variants
Samples
Known GenesTNFSF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182001
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00038


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