A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17176166



Internal ID21623675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51400121..51400121hg38UCSC Ensembl
chr5:50695955..50695955hg19UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5691718
Supporting Variants
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)nssv17176166
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