A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932068



Internal ID22101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26626776..26626906hg38UCSC Ensembl
chr3:26668267..26668397hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449941
Supporting Variants
Samples
Known GenesLRRC3B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932068
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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