A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5705302



Internal ID21731623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32121543..32121543hg38UCSC Ensembl
chr11:32143089..32143089hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17189895
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)nsv5705302
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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