A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072509



Internal ID21484782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111352963..111353018hg38UCSC Ensembl
chr11:111223688..111223743hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600847
Supporting Variants
SamplesNA12329
Known GenesPOU2AF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072509
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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