A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5717502



Internal ID21743823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95373741..95373741hg38UCSC Ensembl
chr15:95916970..95916970hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17248329
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)nsv5717502
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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