A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv727n145



Internal ID22813743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27886488..27887846hg38UCSC Ensembl
chr22:28282476..28283834hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg381359
hg191359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3115466, nsv3113485
Samplessample115, sample229
Known GenesPITPNB
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv727n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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