A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17238598



Internal ID21686107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83629684..83629684hg38UCSC Ensembl
chr15:84298436..84298436hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386016
hg196016
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5722384
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)nssv17238598
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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