A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1356e59



Internal ID22762576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20434985..20447483hg38UCSC Ensembl
chr15:20640238..20652736hg19UCSC Ensembl
chr15:18900252..18912750hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3812499
hg1912499
hg1812499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3347632, esv3449229
SamplesNA19238, NA19239
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1356e59
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