A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv267e59



Internal ID20127016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201006501..201008199hg38UCSC Ensembl
chr1:200975629..200977327hg19UCSC Ensembl
chr1:199242252..199243950hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3410758, esv3412457
SamplesNA19238, NA19240
Known GenesKIF21B
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv267e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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