A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17189503



Internal ID21637012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10333524..10333524hg38UCSC Ensembl
chr11:10355071..10355071hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5710780
Supporting Variants
Samples
Known GenesCAND1.11
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)nssv17189503
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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