A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1956e59



Internal ID20128705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:60001..77450hg38UCSC Ensembl
chr19:60001..77450hg19UCSC Ensembl
chr19:10952..28450hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3817450
hg1917450
hg1817499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3391077, esv3386920
SamplesNA12878, NA12892
Known GenesFAM138A, FAM138F, WASH5P
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1956e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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