A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5717546



Internal ID21743867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24665779..24665779hg38UCSC Ensembl
chrX:24683896..24683896hg19UCSC Ensembl
CytobandXp22.11
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 Variantsnssv17228317
Samples
Known GenesPCYT1B
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)nsv5717546
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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