A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5696267



Internal ID21722588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78550164..78550164hg38UCSC Ensembl
chr8:79462399..79462399hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17184424
Samples
Known GenesPKIA
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)nsv5696267
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