A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931153



Internal ID21521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18561150..18562628hg38UCSC Ensembl
chr3:18602642..18604120hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381479
hg191479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443245
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931153
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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