A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14223717



Internal ID3468981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87331554..87369058hg38UCSC Ensembl
chr11:87042596..87080100hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3837505
hg1937505
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627124
Supporting Variants
SamplesHG03086
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14223717
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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