A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6775633



Internal ID10181551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:106638181..106638331hg38UCSC Ensembl
Outerchr11:106508907..106509057hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745028
Supporting Variants
SamplesSSM066
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)essv6775633
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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