A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2744989



Internal ID9979273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:102399202..102401911hg38UCSC Ensembl
Outerchr11:102269933..102272642hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg382710
hg192710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6735124, essv6735125
SamplesSSM049
Known GenesTMEM123
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2744989
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