A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5718112



Internal ID21744433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19088572..19088572hg38UCSC Ensembl
chr10:19377501..19377501hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17236966
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)nsv5718112
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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