A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4425e59



Internal ID22765645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65259126..65282824hg38UCSC Ensembl
chr9:70152732..70176430hg19UCSC Ensembl
chr9:69442552..69466250hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3823699
hg1923699
hg1823699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3324886, esv3357027, esv3435751, esv3446735
SamplesNA19239, NA12878, NA12892, NA19240
Known GenesFOXD4L5
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4425e59
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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