A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046308



Internal ID18788839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94681543..94873255hg38UCSC Ensembl
Innerchr10:96441300..96633012hg19UCSC Ensembl
Innerchr10:96431290..96623002hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38191713
hg19191713
hg18191713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512803
Samples
Known GenesCYP2C18, CYP2C19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046308
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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