A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621100



Internal ID7007969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93433583..93438085hg38UCSC Ensembl
Innerchr9:93433583..93438085hg38UCSC Ensembl
Outerchr9:93433369..93438319hg38UCSC Ensembl
chr9:96195865..96200367hg19UCSC Ensembl
Innerchr9:96195865..96200367hg19UCSC Ensembl
Outerchr9:96195651..96200601hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg384503
hg194503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13560051, essv13560052
SamplesNA20809, NA19439
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621100
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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