A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16941021



Internal ID28053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:144097574..144103600hg38UCSC Ensembl
chr3:143816416..143822442hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg386027
hg196027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434503
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16941021
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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