A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17236882



Internal ID21684391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:122379150..122379150hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382151
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5714791
Supporting Variants
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)nssv17236882
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