A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8393n54



Internal ID22776288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78866055..78936655hg38UCSC Ensembl
chr3:78915205..78985805hg19UCSC Ensembl
chr3:78997895..79068495hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3870601
hg1970601
hg1870601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590735, nsv590734
Samples
Known GenesROBO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8393n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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