A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16943445



Internal ID29614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174423921..174423972hg38UCSC Ensembl
chr3:174141711..174141762hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5406235
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16943445
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002654


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