A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567358



Internal ID18865639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40854226..40886249hg38UCSC Ensembl
Innerchr19:41360131..41392154hg19UCSC Ensembl
Innerchr19:46051971..46083994hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3832024
hg1932024
hg1832024
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063860
Supporting Variants
Samples
Known GenesCYP2A7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567358
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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