A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5725996



Internal ID21752317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36536940..36536940hg38UCSC Ensembl
chr11:36558490..36558490hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg386018
hg196018
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17235857, nssv17250303
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)nsv5725996
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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