A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627617



Internal ID7014445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105759470..105761992hg38UCSC Ensembl
Innerchr11:105759510..105761952hg38UCSC Ensembl
Outerchr11:105759430..105762032hg38UCSC Ensembl
chr11:105630196..105632718hg19UCSC Ensembl
Innerchr11:105630236..105632678hg19UCSC Ensembl
Outerchr11:105630156..105632758hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg382523
hg192523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14268551
SamplesHG03446
Known GenesGRIA4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627617
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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