A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6949014



Internal ID10055193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:110105995..110106296hg38UCSC Ensembl
Outerchr11:109976720..109977021hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745058
Supporting Variants
SamplesSSM024
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)essv6949014
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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