A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5691918



Internal ID21718239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103928546..103928546hg38UCSC Ensembl
chr3:103647390..103647390hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17208343, nssv17222838
Samples
Known Genes
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5691918
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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