A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17235921



Internal ID21683430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112116581..112116581hg38UCSC Ensembl
chr11:111987304..111987304hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5718770
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)nssv17235921
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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