A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2745282



Internal ID9979566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132071201..132071344hg38UCSC Ensembl
Outerchr11:131941095..131941238hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6688239, essv6702396
SamplesSSM035, SSM039
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)esv2745282
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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