A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11433n54



Internal ID20144857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66125574..66134209hg38UCSC Ensembl
chr7:65590561..65599196hg19UCSC Ensembl
chr7:65227996..65236631hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg388636
hg198636
hg188636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607408, nsv607413
Samples
Known GenesCRCP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11433n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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