A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1073e1



Internal ID6308871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33777074..34581561hg19UCSC Ensembl
chr19:38468914..39273401hg18UCSC Ensembl
chr19:38468914..39273401hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Complex
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv14034, esv579, essv15369, essv9767, essv11295
SamplesNA18863, NA18862
Known GenesCEBPA, CEBPG, CHST8, KCTD15, LOC80054, PEPD
Method
Analysis
Platform
Comments
ReferenceRedon et al 2006
Pubmed ID17122850
Accession Number(s)dgv1073e1
Frequency
Sample Size271
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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