A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061439



Internal ID19150658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40846466..40863792hg38UCSC Ensembl
Innerchr19:41352371..41369697hg19UCSC Ensembl
Innerchr19:46044211..46061537hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3817327
hg1917327
hg1817327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3569399
Samples
Known GenesCYP2A6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061439
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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