A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv955n100



Internal ID20152571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94645539..94757047hg38UCSC Ensembl
chr10:96405296..96516804hg19UCSC Ensembl
chr10:96395286..96506794hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38111509
hg19111509
hg18111509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040106, nsv1037516, nsv1049225, nsv1052478, nsv1040976
Samples
Known GenesCYP2C18
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv955n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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