A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9108n54



Internal ID20142532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68527784..68587178hg38UCSC Ensembl
chr4:69393502..69452896hg19UCSC Ensembl
chr4:69076097..69135491hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3859395
hg1959395
hg1859395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594542, nsv594527, nsv594529, nsv594541, nsv594528, nsv594540
Samples
Known GenesUGT2B17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9108n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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