A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5693382



Internal ID21719703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164214999..164214999hg38UCSC Ensembl
chr5:163642005..163642005hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17229571, nssv17177629
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)nsv5693382
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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