A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5690436



Internal ID21716757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84099256..84099256hg38UCSC Ensembl
chr1:84564939..84564939hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17173341, nssv17205203
Samples
Known GenesPRKACB
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)nsv5690436
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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