A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17220022



Internal ID21667531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33160277..33160277hg38UCSC Ensembl
chr13:33734414..33734414hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5710081
Supporting Variants
Samples
Known GenesSTARD13
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)nssv17220022
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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