A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210035



Internal ID20777075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:80344601..80432500hg38UCSC Ensembl
chr3:80393751..80481650hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3887900
hg1987900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366116
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210035
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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