A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11058818



Internal ID3801311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:83685061..83746680hg38UCSC Ensembl
chr3:83734212..83795831hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3861620
hg1961620
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596798
Supporting Variants
SamplesHG03446
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11058818
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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