A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627625



Internal ID7014453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106106908..106113006hg38UCSC Ensembl
Innerchr11:106106911..106113004hg38UCSC Ensembl
Outerchr11:106106906..106113009hg38UCSC Ensembl
chr11:105977635..105983733hg19UCSC Ensembl
Innerchr11:105977638..105983731hg19UCSC Ensembl
Outerchr11:105977633..105983736hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg386099
hg196099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14269250
SamplesHG03114
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627625
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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