A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851322



Internal ID22626257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122712275..122713673hg38UCSC Ensembl
chr11:122582983..122584381hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg381399
hg191399
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456314, nssv17450317
Samples
Known GenesUBASH3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851322
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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