A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626154



Internal ID7012988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43860473..43861883hg38UCSC Ensembl
Innerchr11:43860511..43861846hg38UCSC Ensembl
Outerchr11:43860436..43861921hg38UCSC Ensembl
chr11:43882023..43883433hg19UCSC Ensembl
Innerchr11:43882061..43883396hg19UCSC Ensembl
Outerchr11:43881986..43883471hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381411
hg191411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14114424, essv14114428, essv14114423, essv14114429, essv14114425, essv14114422, essv14114427, essv14114426
SamplesHG02375, HG00851, HG01848, HG02131, HG01844, HG01796, HG02364, HG01811
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626154
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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