A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026746



Internal ID21936089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134408224..134408545hg38UCSC Ensembl
chr11:134278118..134278439hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614412
Samples
Known GenesB3GAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026746
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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