A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568220



Internal ID18519815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40823313..40891756hg38UCSC Ensembl
Innerchr19:41329218..41397661hg19UCSC Ensembl
Innerchr19:46021058..46089501hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3868444
hg1968444
hg1868444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056244
Supporting Variants
Samples
Known GenesCYP2A6, CYP2A7, CYP2G1P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3568220
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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