A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625783



Internal ID7012617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28373563..28387486hg38UCSC Ensembl
Innerchr11:28374063..28386986hg38UCSC Ensembl
Outerchr11:28372563..28388486hg38UCSC Ensembl
chr11:28395110..28409033hg19UCSC Ensembl
Innerchr11:28395610..28408533hg19UCSC Ensembl
Outerchr11:28394110..28410033hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3813924
hg1913924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14073375, essv14073374
SamplesHG04183, HG03698
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625783
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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