A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv27e59



Internal ID18985528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3693628..3695026hg38UCSC Ensembl
chr1:3610192..3611590hg19UCSC Ensembl
chr1:3600052..3601450hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3382922, esv3432428
SamplesNA19240
Known GenesTP73
MethodSequencing
Analysis
PlatformIllumina
SOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv27e59
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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