A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627198



Internal ID6667346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90283625..90305577hg38UCSC Ensembl
chr11:90016793..90038745hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3821953
hg1921953
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14231042
SamplesNA19756
Known GenesDISC1FP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627198
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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