A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5719087



Internal ID21745408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85027633..85027633hg38UCSC Ensembl
chrX:84282639..84282639hg19UCSC Ensembl
CytobandXq21.1
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 Variantsnssv17205335, nssv17227373
Samples
Known GenesAPOOL
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)nsv5719087
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer