A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1108n145



Internal ID22814124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66125246..66128293hg38UCSC Ensembl
chr7:65590233..65593280hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg383048
hg193048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112681, nsv3111195, nsv3116248
Samplessample322, sample123, sample164, sample202, sample95, sample178, sample345, sample243, sample99
Known GenesCRCP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1108n145
Frequency
Sample Size467
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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