A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17196989



Internal ID21644498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92837505..92837505hg38UCSC Ensembl
chr14:93303850..93303850hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5698374
Supporting Variants
Samples
Known GenesGOLGA5
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)nssv17196989
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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