A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619394



Internal ID6659584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6137627..6254604hg38UCSC Ensembl
chr9:6137627..6254604hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38116978
hg19116978
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13385783
SamplesHG01968
Known GenesIL33
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619394
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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