A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2726720



Internal ID5037452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:853796..854223hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv6918162
SamplesSSM017
Known GenesGAK
Method
Analysis
PlatformIllumina HiSeq2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2726720
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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