A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv412e59



Internal ID20127161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46541973..46556271hg38UCSC Ensembl
chr10:46993346..47007644hg19UCSC Ensembl
chr10:46413352..46427650hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3814299
hg1914299
hg1814299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3336367, esv3447001
SamplesNA12892, NA19238
Known GenesGPRIN2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv412e59
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