A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372321



Internal ID21029874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51926781..51927476hg38UCSC Ensembl
chr3:51960797..51961492hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209979
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372321
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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