A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933232



Internal ID22884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68658856..68658955hg38UCSC Ensembl
chr3:68708007..68708106hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933232
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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