A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047782



Internal ID18790313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94821337..94958722hg38UCSC Ensembl
Innerchr10:96581094..96718479hg19UCSC Ensembl
Innerchr10:96571084..96708469hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38137386
hg19137386
hg18137386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706198
Samples
Known GenesCYP2C19, CYP2C9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047782
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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