A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066928



Internal ID19156147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40842952..40865028hg38UCSC Ensembl
Innerchr19:41348857..41370933hg19UCSC Ensembl
Innerchr19:46040697..46062773hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3822077
hg1922077
hg1822077
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3535n100
Supporting Variantsnssv3568259, nssv3568260, nssv3568258
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)nsv1066928
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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