A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17231929



Internal ID21679438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86330933..86330933hg38UCSC Ensembl
chr11:86041975..86041975hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5704123
Supporting Variants
Samples
Known GenesC11orf73
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)nssv17231929
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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