A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5718942



Internal ID21745263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42920260..42920260hg38UCSC Ensembl
chr11:42941810..42941810hg19UCSC Ensembl
Cytoband11p12
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 Variantsnssv17245612
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)nsv5718942
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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