A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5705074



Internal ID21731395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27427970..27427970hg38UCSC Ensembl
chr22:27823931..27823931hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17202096
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)nsv5705074
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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