A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5702497



Internal ID21728818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:129490626..129490626hg38UCSC Ensembl
chr12:129975171..129975171hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17194331, nssv17226196
Samples
Known GenesTMEM132D
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)nsv5702497
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