A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17179366



Internal ID21626875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168142615..168142615hg38UCSC Ensembl
chr5:167569620..167569620hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5686571
Supporting Variants
Samples
Known GenesTENM2
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)nssv17179366
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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