A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5724829



Internal ID21751150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132057492..132057492hg38UCSC Ensembl
chr3:131776336..131776336hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17242264
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)nsv5724829
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer