A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv342e59



Internal ID20127091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1231812..1233208hg38UCSC Ensembl
chr10:1277752..1279150hg19UCSC Ensembl
chr10:1267752..1269150hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381397
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3331395, esv3426119
SamplesNA19239, NA19240
Known GenesADARB2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv342e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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