A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17211566



Internal ID21659075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183715294..183715294hg38UCSC Ensembl
chr3:183433082..183433082hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5689750
Supporting Variants
Samples
Known GenesYEATS2
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)nssv17211566
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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