A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023718



Internal ID21933061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62618962..62619130hg38UCSC Ensembl
chr11:62386434..62386602hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590270
Samples
Known GenesB3GAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023718
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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