A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620889



Internal ID7007759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82745348..82746957hg38UCSC Ensembl
Innerchr9:82745406..82746899hg38UCSC Ensembl
Outerchr9:82745290..82747015hg38UCSC Ensembl
chr9:85360263..85361872hg19UCSC Ensembl
Innerchr9:85360321..85361814hg19UCSC Ensembl
Outerchr9:85360205..85361930hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381610
hg191610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13538827
SamplesHG03702
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620889
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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