A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5730239



Internal ID21756560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97527572..97527572hg38UCSC Ensembl
chr14:97993909..97993909hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38895
hg19895
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17252856, nssv17246422
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)nsv5730239
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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