A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5716639



Internal ID21742960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3592013..3592013hg38UCSC Ensembl
chrX:3510054..3510054hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg381003
hg191003
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17250899
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)nsv5716639
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