A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627686



Internal ID7014514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108807304..108839460hg38UCSC Ensembl
chr11:108678031..108710187hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3832157
hg1932157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14278430, essv14278431
SamplesHG03668, HG00234
Known GenesDDX10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627686
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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