A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209575



Internal ID20776615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134052374..134071221hg38UCSC Ensembl
chr3:133771218..133790065hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3818848
hg1918848
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363009
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209575
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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