A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5722122



Internal ID21748443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155282341..155282341hg38UCSC Ensembl
chrX:154511630..154511630hg19UCSC Ensembl
CytobandXq28
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 Variantsnssv17203557, nssv17223186
Samples
Known GenesCLIC2
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)nsv5722122
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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