A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17223656



Internal ID21671165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46619669..46619669hg38UCSC Ensembl
chr19:47122926..47122926hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5697551
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)nssv17223656
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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