A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5710642



Internal ID21736963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67055007..67055007hg38UCSC Ensembl
chr10:68814765..68814765hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17188596
Samples
Known GenesCTNNA3, LRRTM3
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)nsv5710642
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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