A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8782n54



Internal ID22776677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189647635..189652165hg38UCSC Ensembl
chr3:189365424..189369954hg19UCSC Ensembl
chr3:190848118..190852648hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg384531
hg194531
hg184531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592783, nsv592778, nsv592782
Samples
Known GenesTP63
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8782n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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