A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1957e59



Internal ID20128706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:60001..86350hg38UCSC Ensembl
chr19:60001..86350hg19UCSC Ensembl
chr19:10952..37350hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3826350
hg1926350
hg1826399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3383845, esv3337337
SamplesNA19238, NA19240
Known GenesFAM138A, FAM138F, WASH5P
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1957e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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