A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5720143



Internal ID21746464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:196216360..196216360hg38UCSC Ensembl
chr2:197081084..197081084hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg386010
hg196010
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17233875
Samples
Known GenesHECW2
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)nsv5720143
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