A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143789



Internal ID342990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90076896..90092000hg38UCSC Ensembl
chr11:89810064..89825168hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3815105
hg1915105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050851
Samples
Known GenesUBTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143789
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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