A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1793e59



Internal ID22763013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64899272..64904270hg38UCSC Ensembl
chr17:62895390..62900388hg19UCSC Ensembl
chr17:60325852..60330850hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg384999
hg194999
hg184999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3411544, esv3448945
SamplesNA12891, NA12878
Known GenesLRRC37A3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1793e59
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