A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11097278



Internal ID3757358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108762663..108863577hg38UCSC Ensembl
chr3:108481510..108582424hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38100915
hg19100915
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597330
Supporting Variants
SamplesHG03388
Known GenesTRAT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11097278
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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