A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5725018



Internal ID21751339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118702850..118702850hg38UCSC Ensembl
chrX:117836813..117836813hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17205438
Samples
Known Genes
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)nsv5725018
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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