A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17244192



Internal ID21691701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13937639..13937639hg38UCSC Ensembl
chr9:13937638..13937638hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg382676
hg192676
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5724904
Supporting Variants
Samples
Known GenesLINC00583
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)nssv17244192
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