A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044182



Internal ID18786713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95024239..95054932hg38UCSC Ensembl
Innerchr10:96783996..96814689hg19UCSC Ensembl
Innerchr10:96773986..96804679hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3830694
hg1930694
hg1830694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513958
Samples
Known GenesCYP2C8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044182
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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