A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6924278



Internal ID9686960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:131928431..131928869hg38UCSC Ensembl
Outerchr11:131798325..131798763hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745273
Supporting Variants
SamplesSSM018
Known GenesNTM
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)essv6924278
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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