A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14320169



Internal ID6502870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133785215..133829890hg38UCSC Ensembl
chr11:133655110..133699785hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3844676
hg1944676
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628158
Supporting Variants
SamplesNA20534
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14320169
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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