A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3539n100



Internal ID22789626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40846466..40891756hg38UCSC Ensembl
chr19:41352371..41397661hg19UCSC Ensembl
chr19:46044211..46089501hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3845291
hg1945291
hg1845291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056686, nsv1066009, nsv1061654, nsv1064217, nsv1062790, nsv1060398, nsv1055263, nsv1060679
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)dgv3539n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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