A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6834836



Internal ID9887961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132069893..132070185hg38UCSC Ensembl
Outerchr11:131939787..131940079hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745280, esv2745278
Supporting Variants
SamplesSSM082
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)essv6834836
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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