A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5682799



Internal ID21709120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55865585..55865585hg38UCSC Ensembl
chr4:56731751..56731751hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17221782
Samples
Known GenesEXOC1
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)nsv5682799
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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