A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5689186



Internal ID21715507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135545278..135545278hg38UCSC Ensembl
chr5:134880968..134880968hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17177465
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)nsv5689186
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