A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097555



Internal ID22006788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134408208..134408208hg38UCSC Ensembl
chr11:134278102..134278102hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609743
Samples
Known GenesB3GAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097555
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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