A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5727464



Internal ID21753785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:129990203..129990203hg38UCSC Ensembl
chr8:131002449..131002449hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17246074
Samples
Known GenesFAM49B
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)nsv5727464
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