A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17240106



Internal ID21687615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:36339991..36339991hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384477
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5721298
Supporting Variants
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)nssv17240106
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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