A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627688



Internal ID7014516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108895066..109029952hg38UCSC Ensembl
chr11:108765793..108900679hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38134887
hg19134887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14278455
SamplesHG03668
Known GenesDDX10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627688
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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