A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944372



Internal ID30253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188849332..188849332hg38UCSC Ensembl
chr3:188567120..188567120hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412012
Supporting Variants
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944372
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005322


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