A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369359



Internal ID21026912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31342123..31365494hg38UCSC Ensembl
chr3:31383615..31406986hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3823372
hg1923372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210505
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369359
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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