A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6446n54



Internal ID22774341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40848628..40878673hg38UCSC Ensembl
chr19:41354533..41384578hg19UCSC Ensembl
chr19:46046373..46076418hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3830046
hg1930046
hg1830046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579566, nsv579555, nsv579558, nsv579539, nsv579554, nsv579567, nsv579546, nsv579563, nsv579575, nsv579562, nsv579568, nsv579564, nsv579574, nsv579552, nsv579540, nsv579570, nsv579571, nsv579560, nsv579559, nsv579551, nsv579572, nsv579544, nsv579553, nsv579561, nsv579573
Samples
Known GenesCYP2A6, CYP2A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6446n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss56
Observed Complex0
Frequencyn/a


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