A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627667



Internal ID7014495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107917553..107934434hg38UCSC Ensembl
chr11:107788279..107805160hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3816882
hg1916882
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14277722
SamplesHG02049
Known GenesRAB39A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627667
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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