A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627735



Internal ID7014563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111344399..111349850hg38UCSC Ensembl
Innerchr11:111344399..111349850hg38UCSC Ensembl
Outerchr11:111344203..111350045hg38UCSC Ensembl
chr11:111215124..111220575hg19UCSC Ensembl
Innerchr11:111215124..111220575hg19UCSC Ensembl
Outerchr11:111214928..111220770hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg385452
hg195452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14286898
SamplesNA18560
Known GenesMIR4491
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627735
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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