A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6936022



Internal ID10045010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:76692585..76692790hg38UCSC Ensembl
Outerchr11:76403629..76403834hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744793
Supporting Variants
SamplesSSM021
Known GenesGUCY2EP
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)essv6936022
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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