A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1723e59



Internal ID22762943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:26963199..26984197hg38UCSC Ensembl
chr17:25290225..25311223hg19UCSC Ensembl
chr17:22314352..22335350hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3820999
hg1920999
hg1820999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3332077, esv3356636
SamplesNA12891, NA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1723e59
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