A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6912520



Internal ID10021882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:110155954..110156334hg38UCSC Ensembl
Outerchr11:110026679..110027059hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745059, esv2745060
Supporting Variants
SamplesSSM015
Known GenesZC3H12C
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)essv6912520
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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