A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17239078



Internal ID21686587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81721235..81721235hg38UCSC Ensembl
chr3:81770386..81770386hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5714355
Supporting Variants
Samples
Known GenesGBE1
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)nssv17239078
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