A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925385



Internal ID22700612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122673960..122674068hg38UCSC Ensembl
chr11:122544668..122544776hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369049
Samples
Known GenesUBASH3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925385
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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