A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625459



Internal ID7012293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16886246..16909481hg38UCSC Ensembl
chr11:16907793..16931028hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3823236
hg1923236
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14037351, essv14037350, essv14037352, essv14037353
SamplesNA19057, NA19068, NA18956, NA19011
Known GenesPLEKHA7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625459
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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