A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035409



Internal ID18777940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94735420..95072300hg38UCSC Ensembl
Innerchr10:96495177..96832057hg19UCSC Ensembl
Innerchr10:96485167..96822047hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38336881
hg19336881
hg18336881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503710
Samples
Known GenesCYP2C18, CYP2C19, CYP2C8, CYP2C9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035409
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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