A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6740933



Internal ID9802267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:36756303..36756624hg38UCSC Ensembl
Outerchr11:36777853..36778174hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744351, esv2744349, esv2744350
Supporting Variants
SamplesSSM052
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)essv6740933
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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