A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17184163



Internal ID21631672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21303778..21303778hg38UCSC Ensembl
chr8:21161289..21161289hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5706610
Supporting Variants
Samples
Known GenesLOC101929172
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)nssv17184163
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