A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3531n100



Internal ID22789618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40828821..40875029hg38UCSC Ensembl
chr19:41334726..41380934hg19UCSC Ensembl
chr19:46026566..46072774hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3846209
hg1946209
hg1846209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066884, nsv1059038, nsv1057349, nsv1058747, nsv1058732, nsv1057412, nsv1066701, nsv1063224, nsv1064519, nsv1055204, nsv1062369
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)dgv3531n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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