A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032125



Internal ID21941468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117926091..117926205hg38UCSC Ensembl
chr11:117796806..117796920hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602143
Samples
Known GenesTMPRSS13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032125
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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