A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17215099



Internal ID21662608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50111090..50111090hg38UCSC Ensembl
chr1:50576762..50576762hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5685721
Supporting Variants
Samples
Known GenesELAVL4
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)nssv17215099
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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