A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5721780



Internal ID21748101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:66548026..66548026hg38UCSC Ensembl
chrX:65767868..65767868hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17230397
Samples
Known Genes
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a L1 mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5721780
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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