A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5728631



Internal ID21754952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:18731386..18731386hg38UCSC Ensembl
chrX:18749504..18749504hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17204265, nssv17217025
Samples
Known GenesPPEF1
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)nsv5728631
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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