A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17252659



Internal ID21700168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95210044..95210044hg38UCSC Ensembl
chr15:95753273..95753273hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38776
hg19776
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5721834
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)nssv17252659
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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