A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6908811



Internal ID9671921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:134281595..134344521hg38UCSC Ensembl
Outerchr11:134151489..134214415hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3862927
hg1962927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745325
Supporting Variants
SamplesSSM014
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)essv6908811
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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