A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5716637



Internal ID21742958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9851458..9851458hg38UCSC Ensembl
chr11:9873005..9873005hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383163
hg193163
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17233793
Samples
Known GenesSBF2
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)nsv5716637
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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