A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17220015



Internal ID21667524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111195581..111195581hg38UCSC Ensembl
chr3:110914428..110914428hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5685370
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)nssv17220015
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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