A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5718775



Internal ID21745096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10001895..10001895hg38UCSC Ensembl
chr8:9859405..9859405hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17233372
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)nsv5718775
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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