A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937282



Internal ID25573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86652293..86746783hg38UCSC Ensembl
chr3:86701443..86795933hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3894491
hg1994491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453813
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937282
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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