A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv726n145



Internal ID22813742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27794964..27803115hg38UCSC Ensembl
chr22:28190952..28199103hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg388152
hg198152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116985, nsv3112341
Samplessample373, sample363
Known GenesMN1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv726n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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