A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730129



Internal ID153795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28798672..28798672hg38UCSC Ensembl
chr3:28840163..28840163hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5410273
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730129
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.209563


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