A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5679371



Internal ID21705692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42507518..42507518hg38UCSC Ensembl
chr2:42734658..42734658hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17199797
Samples
Known GenesMTA3
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)nsv5679371
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