A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065684



Internal ID18808215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41010484..41138637hg38UCSC Ensembl
Innerchr19:41516389..41644542hg19UCSC Ensembl
Innerchr19:46208229..46336382hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38128154
hg19128154
hg18128154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722780
Samples
Known GenesCYP2A13, CYP2B6, CYP2F1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065684
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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