A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620824



Internal ID7007694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79292472..79294818hg38UCSC Ensembl
Innerchr9:79292472..79294818hg38UCSC Ensembl
Outerchr9:79292379..79294992hg38UCSC Ensembl
chr9:81907387..81909733hg19UCSC Ensembl
Innerchr9:81907387..81909733hg19UCSC Ensembl
Outerchr9:81907294..81909907hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg382347
hg192347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13534722, essv13534723
SamplesHG01072, HG00731
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620824
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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