A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628142



Internal ID6668286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133122279..133134578hg38UCSC Ensembl
Innerchr11:133122279..133134578hg38UCSC Ensembl
Outerchr11:133122056..133134721hg38UCSC Ensembl
chr11:132992174..133004473hg19UCSC Ensembl
Innerchr11:132992174..133004473hg19UCSC Ensembl
Outerchr11:132991951..133004616hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3812300
hg1912300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14318167, essv14318163, essv14318164, essv14318165, essv14318166, essv14318168
SamplesHG01441, HG04209, NA12400, HG00640, NA12283, HG01939
Known GenesOPCML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628142
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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