A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568254



Internal ID18866535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40839241..40875029hg38UCSC Ensembl
Innerchr19:41345146..41380934hg19UCSC Ensembl
Innerchr19:46036986..46072774hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3835789
hg1935789
hg1835789
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067231
Supporting Variants
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)nssv3568254
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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