A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1355n54



Internal ID18993531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94684492..94930614hg38UCSC Ensembl
chr10:96444249..96690371hg19UCSC Ensembl
chr10:96434239..96680361hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38246123
hg19246123
hg18246123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551957, nsv551955, nsv551956
Samples
Known GenesCYP2C18, CYP2C19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1355n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer