A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17197590



Internal ID21645099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79126715..79126715hg38UCSC Ensembl
chr15:79419057..79419057hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5701236
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)nssv17197590
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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