A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5721043



Internal ID21747364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188117521..188117521hg38UCSC Ensembl
chr3:187835309..187835309hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17241684
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)nsv5721043
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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