A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5728218



Internal ID21754539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14069306..14069306hg38UCSC Ensembl
chr9:14069305..14069305hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17240955
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)nsv5728218
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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