A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9104n54



Internal ID20142528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68509002..68661688hg38UCSC Ensembl
chr4:69374720..69527406hg19UCSC Ensembl
chr4:69057315..69210001hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38152687
hg19152687
hg18152687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594512, nsv594510, nsv594511, nsv594525
Samples
Known GenesUGT2B15, UGT2B17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9104n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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