A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9181n54



Internal ID20142605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101039102..101040790hg38UCSC Ensembl
chr4:101960259..101961947hg19UCSC Ensembl
chr4:102179282..102180970hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381689
hg191689
hg181689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594952, nsv594949
Samples
Known GenesPPP3CA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9181n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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