A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17213382



Internal ID21660891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:130980099..130980099hg38UCSC Ensembl
chr12:131464644..131464644hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5703642
Supporting Variants
Samples
Known GenesGPR133
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)nssv17213382
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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