A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17173935



Internal ID21621444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89046133..89046133hg38UCSC Ensembl
chr1:89511816..89511816hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5675054
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)nssv17173935
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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