A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035728



Internal ID21945071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122662159..122662682hg38UCSC Ensembl
chr11:122532867..122533390hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611125
Samples
Known GenesUBASH3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035728
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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