A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5717054



Internal ID21743375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119596014..119596014hg38UCSC Ensembl
chr5:118931709..118931709hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg385283
hg195283
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17234698
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)nsv5717054
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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