A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17190350



Internal ID21637859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12982927..12982927hg38UCSC Ensembl
chr11:13004474..13004474hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5713176
Supporting Variants
Samples
Known GenesLINC00958
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)nssv17190350
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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