A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621036



Internal ID7007906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89916560..89964059hg38UCSC Ensembl
chr9:92678842..92726341hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3847500
hg1947500
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13552294
SamplesNA20318
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621036
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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