A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933646



Internal ID23165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42464971..42465045hg38UCSC Ensembl
chr3:42506463..42506537hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446623
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933646
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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