A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8783n54



Internal ID20142207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189649531..189653225hg38UCSC Ensembl
chr3:189367320..189371014hg19UCSC Ensembl
chr3:190850014..190853708hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg383695
hg193695
hg183695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592786, nsv592785
Samples
Known GenesTP63
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8783n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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