A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5725357



Internal ID21751678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72899395..72899395hg38UCSC Ensembl
chr15:73191736..73191736hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17242328, nssv17236730
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)nsv5725357
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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