A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2747380



Internal ID5058112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:49002242..49002549hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv6970987, essv6823786, essv6851454, essv6966049, essv6867098, essv6928054, essv6815590, essv6924493, essv6932012, essv6688221, essv6775845, essv6897750, essv6940362, essv6977510, essv6744136, essv6916272, essv6673395, essv6720831, essv6809501
SamplesSSM027, SSM053, SSM086, SSM099, SSM031, SSM020, SSM016, SSM077, SSM005, SSM011, SSM066, SSM028, SSM029, SSM003, SSM019, SSM079, SSM044, SSM075, SSM018
Known GenesLPAR6, RB1
Method
Analysis
PlatformIllumina HiSeq2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2747380
Frequency
Sample Size96
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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