A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13691146



Internal ID21213003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111358302..111358383hg38UCSC Ensembl
chr11:111229027..111229108hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789719
Supporting Variants
Samples
Known GenesPOU2AF1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13691146
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.725806


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