A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483424



Internal ID21140977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71232401..71283600hg38UCSC Ensembl
chr13:71806533..71857732hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3851200
hg1951200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1912n223
Supporting Variantsnssv18179243
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483424
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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