A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5693193



Internal ID21719514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53578935..53578935hg38UCSC Ensembl
chr4:54445102..54445102hg19UCSC 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 Variantsnssv17211137, nssv17216939
Samples
Known GenesLNX1
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)nsv5693193
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer