A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv344e59



Internal ID20127093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1396657..1398355hg38UCSC Ensembl
chr10:1438852..1440550hg19UCSC Ensembl
chr10:1428852..1430550hg18UCSC Ensembl
Cytoband10p15.3
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 Variantsesv3378006, esv3359704
SamplesNA19239, NA19240
Known GenesADARB2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv344e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer