A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621418



Internal ID7008287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108209589..108211805hg38UCSC Ensembl
Innerchr9:108209596..108211799hg38UCSC Ensembl
Outerchr9:108209583..108211812hg38UCSC Ensembl
chr9:110971869..110974085hg19UCSC Ensembl
Innerchr9:110971876..110974079hg19UCSC Ensembl
Outerchr9:110971863..110974092hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382217
hg192217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13594830
SamplesNA19397
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621418
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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