A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6442n54



Internal ID22774337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40843827..40887855hg38UCSC Ensembl
chr19:41349732..41393760hg19UCSC Ensembl
chr19:46041572..46085600hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3844029
hg1944029
hg1844029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579528, nsv579534, nsv579548, nsv579526, nsv579549, nsv579556, nsv579532
Samples
Known GenesCYP2A6, CYP2A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6442n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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