A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17191841



Internal ID21639350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95203161..95203161hg38UCSC Ensembl
chr11:94936325..94936325hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5713145
Supporting Variants
Samples
Known GenesSESN3
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)nssv17191841
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