A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6449n54



Internal ID22774344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40856268..40877894hg38UCSC Ensembl
chr19:41362173..41383799hg19UCSC Ensembl
chr19:46054013..46075639hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3821627
hg1921627
hg1821627
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579584, nsv579578
Samples
Known GenesCYP2A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6449n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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