A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5699077



Internal ID21725398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39340387..39340387hg38UCSC Ensembl
chr22:39736392..39736392hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17221440, nssv17204210
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)nsv5699077
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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