A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17228234



Internal ID21675743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102642303..102642303hg38UCSC Ensembl
chr11:102513034..102513034hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5711274
Supporting Variants
Samples
Known Genes
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)nssv17228234
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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