A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6787698



Internal ID9845160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:124109319..124109438hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745183, esv2745180
Supporting Variants
SamplesSSM069
Known Genes
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)essv6787698
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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