A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5703746



Internal ID21730067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57650230..57650230hg38UCSC Ensembl
chr20:56225286..56225286hg19UCSC Ensembl
Cytoband20q13.31
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 Variantsnssv17202620
Samples
Known GenesPMEPA1
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)nsv5703746
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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