A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568253



Internal ID18866534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40839241..40865028hg38UCSC Ensembl
Innerchr19:41345146..41370933hg19UCSC Ensembl
Innerchr19:46036986..46062773hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3825788
hg1925788
hg1825788
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058924
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)nssv3568253
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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