A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5717231



Internal ID21743552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35814850..35814850hg38UCSC Ensembl
chr11:35836400..35836400hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg386016
hg196016
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17247100
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)nsv5717231
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