A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17201166



Internal ID21648675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37810821..37810821hg38UCSC Ensembl
chr2:38037964..38037964hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5688629
Supporting Variants
Samples
Known Genes
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)nssv17201166
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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