A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936991



Internal ID25372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94347640..94351602hg38UCSC Ensembl
chr3:94066484..94070446hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg383963
hg193963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936991
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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