A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5706061



Internal ID21732382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42014404..42014404hg38UCSC Ensembl
chr21:43434513..43434513hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17233040, nssv17203733
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)nsv5706061
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