A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936223



Internal ID24873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81114430..81171365hg38UCSC Ensembl
chr3:81163581..81220516hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3856936
hg1956936
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446922
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936223
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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