A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114263



Internal ID21297529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:44725421..44747096hg38UCSC Ensembl
Innerchr22:45121301..45142976hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3821676
hg1921676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14103011
Samplessample275
Known GenesPRR5, PRR5-ARHGAP8
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114263
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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