A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13409952



Internal ID5489425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16058917..16096870hg38UCSC Ensembl
chr9:16058915..16096868hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3837954
hg1937954
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619804
Supporting Variants
SamplesNA18981
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13409952
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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