A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17175113



Internal ID21622622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:20306381..20306381hg38UCSC Ensembl
chr5:20306490..20306490hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5686421
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)nssv17175113
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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