A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9151n54



Internal ID20142575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86057916..86058774hg38UCSC Ensembl
chr4:86979069..86979927hg19UCSC Ensembl
chr4:87198093..87198951hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38859
hg19859
hg18859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594785, nsv594784, nsv594783
SamplesNINDS_100, HGDP01033, HGDP00994, HGDP00643, HGDP00627
Known GenesMAPK10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9151n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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