A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17225223



Internal ID21672732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41311988..41311988hg38UCSC Ensembl
chr3:41353479..41353479hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5681262
Supporting Variants
Samples
Known GenesULK4
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17225223
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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