A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16942163



Internal ID28793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169042103..169042956hg38UCSC Ensembl
chr3:168759891..168760744hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435466
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16942163
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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