A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17195322



Internal ID21642831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91242251..91242251hg38UCSC Ensembl
chr13:91894505..91894505hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5697225
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)nssv17195322
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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