A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1356n54



Internal ID18993532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94736036..94797579hg38UCSC Ensembl
chr10:96495793..96557336hg19UCSC Ensembl
chr10:96485783..96547326hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3861544
hg1961544
hg1861544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551961, nsv551960, nsv551959, nsv551958
Samples
Known GenesCYP2C18, CYP2C19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1356n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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