A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481180



Internal ID21138733
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 StatusM
Merged Variants
Supporting Variantsnssv18182001
Samples
Known GenesTNFSF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481180
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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