A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5698256



Internal ID21724577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15618533..15618533hg38UCSC Ensembl
chr11:15640079..15640079hg19UCSC Ensembl
Cytoband11p15.2
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 Variantsnssv17229774, nssv17190384
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)nsv5698256
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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