A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv64e59



Internal ID20126813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22577572..22580170hg38UCSC Ensembl
chr1:22904065..22906663hg19UCSC Ensembl
chr1:22776652..22779250hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg382599
hg192599
hg182599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3382026, esv3437457
SamplesNA19238, NA19240
Known GenesEPHA8
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv64e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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