A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5700337



Internal ID21726658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78735306..78735306hg38UCSC Ensembl
chr8:79647541..79647541hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17184430
Samples
Known GenesIL7
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)nsv5700337
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