A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032268



Internal ID21941611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134408214..134408356hg38UCSC Ensembl
chr11:134278108..134278250hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602198
Samples
Known GenesB3GAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032268
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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