A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5686557



Internal ID21712878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87857649..87857649hg38UCSC Ensembl
chr5:87153466..87153466hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17213194, nssv17177823
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)nsv5686557
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