A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5725841



Internal ID21752162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:8042164..8042164hg38UCSC Ensembl
chr20:8022811..8022811hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg386016
hg196016
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17252602
Samples
Known Genes
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a L1 mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5725841
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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