A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17202780



Internal ID21650289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3261772..3261772hg38UCSC Ensembl
chr20:3242418..3242418hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5699908
Supporting Variants
Samples
Known GenesC20orf194
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)nssv17202780
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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