A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5689974



Internal ID21716295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231457410..231457410hg38UCSC Ensembl
chr2:232322121..232322121hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17221335, nssv17210252
Samples
Known GenesNCL
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)nsv5689974
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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