A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17220490



Internal ID21667999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53820097..53820097hg38UCSC Ensembl
chr3:53854124..53854124hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5692573
Supporting Variants
Samples
Known GenesCHDH
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)nssv17220490
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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