A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5694426



Internal ID21720747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41689575..41689575hg38UCSC Ensembl
chr19:42193496..42193496hg19UCSC Ensembl
Cytoband19q13.2
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 Variantsnssv17225007, nssv17202768
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)nsv5694426
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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