A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5703829



Internal ID21730150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20360048..20360048hg38UCSC Ensembl
chr20:20340692..20340692hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17202845
Samples
Known GenesC20orf26
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)nsv5703829
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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