A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5678042



Internal ID21704363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119214138..119214138hg38UCSC Ensembl
chr4:120135293..120135293hg19UCSC Ensembl
Cytoband4q26
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 Variantsnssv17175517
Samples
Known GenesUSP53
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)nsv5678042
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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