A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932412



Internal ID22327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33078054..33078939hg38UCSC Ensembl
chr3:33119546..33120431hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38886
hg19886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442795
Supporting Variants
Samples
Known GenesGLB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932412
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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