A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17218374



Internal ID21665883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31395755..31395755hg38UCSC Ensembl
chr15:31687958..31687958hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5710877
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)nssv17218374
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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