A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931889



Internal ID21987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41474613..41745773hg38UCSC Ensembl
chr3:41516104..41787265hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38271161
hg19271162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440654
Supporting Variants
Samples
Known GenesULK4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931889
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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