A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5695599



Internal ID21721920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20508723..20508723hg38UCSC Ensembl
chr14:20976882..20976882hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17194664
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)nsv5695599
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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