A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485159



Internal ID21142712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:62211401..62213400hg38UCSC Ensembl
chr13:62785534..62787533hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485159
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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