A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16942525



Internal ID29022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182606809..182606860hg38UCSC Ensembl
chr3:182324597..182324648hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5398586
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16942525
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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