A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627145



Internal ID7013975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88213886..88232703hg38UCSC Ensembl
Innerchr11:88213886..88232703hg38UCSC Ensembl
Outerchr11:88213672..88232935hg38UCSC Ensembl
chr11:87947054..87965871hg19UCSC Ensembl
Innerchr11:87947054..87965871hg19UCSC Ensembl
Outerchr11:87946840..87966103hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3818818
hg1918818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14224214, essv14224215, essv14224209, essv14224206, essv14224210, essv14224204, essv14224212, essv14224211, essv14224203, essv14224205, essv14224208, essv14224213, essv14224207
SamplesNA21127, HG03772, NA21137, NA21103, HG03832, HG02737, HG03861, HG04162, NA20875, NA21088, HG04209, HG03931, HG04198
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627145
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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