A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5570511



Internal ID9096360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114938105..114949754hg38UCSC Ensembl
chr3:114656952..114668601hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3811650
hg1911650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670295
Supporting Variants
SamplesHG01079
Known GenesZBTB20
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5570511
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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