A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17202645



Internal ID21650154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60688960..60688960hg38UCSC Ensembl
chr20:59264018..59264018hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5703919
Supporting Variants
Samples
Known Genes
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)nssv17202645
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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