A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5727044



Internal ID21753365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73204618..73204618hg38UCSC Ensembl
chr11:72915663..72915663hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381615
hg191615
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17250606
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)nsv5727044
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