A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5696042



Internal ID21722363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36597793..36597793hg38UCSC Ensembl
chr14:37066998..37066998hg19UCSC Ensembl
Cytoband14q13.3
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 Variantsnssv17194731
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)nsv5696042
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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