A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16942435



Internal ID28963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169739898..169757349hg38UCSC Ensembl
chr3:169457686..169475137hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3817452
hg1917452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452566
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16942435
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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