A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17224984



Internal ID21672493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128195896..128195896hg38UCSC Ensembl
chr10:129994160..129994160hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5713334
Supporting Variants
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)nssv17224984
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