A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5715147



Internal ID21741468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132323457..132323457hg38UCSC Ensembl
chr3:132042301..132042301hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17245938
Samples
Known GenesACPP
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)nsv5715147
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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