A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6865197



Internal ID9661832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:134281586..134344429hg38UCSC Ensembl
Outerchr11:134151480..134214323hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3862844
hg1962844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745325
Supporting Variants
SamplesSSM011
Known GenesGLB1L2, GLB1L3
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)essv6865197
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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