A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17239867



Internal ID21687376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112845601..112845601hg38UCSC Ensembl
chr5:112181298..112181298hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg386016
hg196016
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5723998
Supporting Variants
Samples
Known GenesAPC
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)nssv17239867
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