A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5695790



Internal ID21722111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76166351..76166351hg38UCSC Ensembl
chr9:78781267..78781267hg19UCSC Ensembl
Cytoband9q21.13
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 Variantsnssv17187429
Samples
Known GenesPCSK5
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)nsv5695790
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