A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17196119



Internal ID21643628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58911583..58911583hg38UCSC Ensembl
chr15:59203782..59203782hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5702125
Supporting Variants
Samples
Known GenesSLTM
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)nssv17196119
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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