A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5722330



Internal ID21748651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189124836..189124836hg38UCSC Ensembl
chr3:188842625..188842625hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg386018
hg196018
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17249527, nssv17250237
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)nsv5722330
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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