A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621116



Internal ID7007985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94254422..94255254hg38UCSC Ensembl
Innerchr9:94254467..94255210hg38UCSC Ensembl
Outerchr9:94254378..94255299hg38UCSC Ensembl
chr9:97016704..97017536hg19UCSC Ensembl
Innerchr9:97016749..97017492hg19UCSC Ensembl
Outerchr9:97016660..97017581hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13567292
SamplesHG01848
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621116
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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