A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8779n54



Internal ID22776674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189647176..189650568hg38UCSC Ensembl
chr3:189364965..189368357hg19UCSC Ensembl
chr3:190847659..190851051hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg383393
hg193393
hg183393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592768, nsv592766, nsv592767, nsv592769
Samples
Known GenesTP63
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8779n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss50
Observed Complex0
Frequencyn/a


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