A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5727758



Internal ID21754079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87901297..87901297hg38UCSC Ensembl
chr3:87950447..87950447hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17237477
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)nsv5727758
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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