A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5728884



Internal ID21755205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43335405..43335405hg38UCSC Ensembl
chr11:43356955..43356955hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17247400, nssv17234815
Samples
Known GenesAPI5
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)nsv5728884
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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