A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3414e59



Internal ID20130163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159922667..159924365hg38UCSC Ensembl
chr5:159349674..159351372hg19UCSC Ensembl
chr5:159282252..159283950hg18UCSC Ensembl
Cytoband5q33.3
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 Variantsesv3379992, esv3410932
SamplesNA12892, NA12878
Known GenesADRA1B
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3414e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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