A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5723799



Internal ID21750120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24593484..24593484hg38UCSC Ensembl
chrX:24611601..24611601hg19UCSC Ensembl
CytobandXp22.11
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 Variantsnssv17203856
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)nsv5723799
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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