A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11155329



Internal ID4478449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133910127..133921881hg38UCSC Ensembl
chr3:133628971..133640725hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3811755
hg1911755
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597848
Supporting Variants
SamplesHG03977
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11155329
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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