A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv139e55



Internal ID20126618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33406261..34032878hg38UCSC Ensembl
chr19:33897167..34523783hg19UCSC Ensembl
chr19:38589007..39215623hg18UCSC Ensembl
chr19:38589007..39215623hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38626618
hg19626617
hg18626617
hg17626617
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34628, esv34290
SamplesNA18862, NA18863
Known GenesCHST8, KCTD15, PEPD
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv139e55
Frequency
Sample Size771
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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