A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619862



Internal ID7006736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17997361..18281756hg38UCSC Ensembl
chr9:17997359..18281754hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38284396
hg19284396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13415059
SamplesNA20795
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619862
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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