A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089721



Internal ID21270241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4865198..5054417hg38UCSC Ensembl
Innerchr9:4865198..5054417hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38189220
hg19189220
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110705
Supporting Variants
Samplessample148
Known GenesJAK2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089721
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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