A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17220773



Internal ID21668282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134264708..134264708hg38UCSC Ensembl
chr11:134134602..134134602hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5711338
Supporting Variants
Samples
Known GenesACAD8
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)nssv17220773
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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