A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5702380



Internal ID21728701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58664862..58664862hg38UCSC Ensembl
chr14:59131580..59131580hg19UCSC Ensembl
Cytoband14q23.1
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 Variantsnssv17196567, nssv17218942
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)nsv5702380
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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