A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5679285



Internal ID21705606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193645116..193645116hg38UCSC Ensembl
chr3:193362905..193362905hg19UCSC Ensembl
Cytoband3q29
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 Variantsnssv17220584
Samples
Known GenesOPA1
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)nsv5679285
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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