A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv521e59



Internal ID22761741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125885593..125928391hg38UCSC Ensembl
chr10:127574162..127616960hg19UCSC Ensembl
chr10:127564152..127606950hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3842799
hg1942799
hg1842799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3397624, esv3418815, esv3347350, esv3434868, esv3418667, esv3396440
SamplesNA12891, NA19238, NA19239, NA12878, NA12892, NA19240
Known GenesFANK1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv521e59
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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