A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17239665



Internal ID21687174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95373754..95373754hg38UCSC Ensembl
chr15:95916983..95916983hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5720969
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)nssv17239665
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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