A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17228379



Internal ID21675888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34621043..34621043hg38UCSC Ensembl
chr20:33208847..33208847hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5695099
Supporting Variants
Samples
Known GenesPIGU
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)nssv17228379
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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