A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv603n145



Internal ID22813619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28887003..28894788hg38UCSC Ensembl
chr2:29109869..29117654hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg387786
hg197786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114909, nsv3110701
Samplessample294, sample365
Known GenesWDR43
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv603n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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