A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17251856



Internal ID21699365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123367364..123367364hg38UCSC Ensembl
chr10:125126880..125126880hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5724923
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)nssv17251856
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