A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17227123



Internal ID21674632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151409224..151409224hg38UCSC Ensembl
chr3:151127012..151127012hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5677997
Supporting Variants
Samples
Known GenesMED12L
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)nssv17227123
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