A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11068074



Internal ID4509875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89034270..89037367hg38UCSC Ensembl
Innerchr3:89034299..89037339hg38UCSC Ensembl
Outerchr3:89034242..89037396hg38UCSC Ensembl
chr3:89083420..89086517hg19UCSC Ensembl
Innerchr3:89083449..89086489hg19UCSC Ensembl
Outerchr3:89083392..89086546hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg383098
hg193098
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596942
Supporting Variants
SamplesHG04014
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11068074
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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