A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17244888



Internal ID21692397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:91534574..91534574hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38398
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5724740
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)nssv17244888
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