A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088149



Internal ID21284596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21347654..21386358hg38UCSC Ensembl
Innerchr9:21347653..21386357hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3838705
hg1938705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116598
Supporting Variants
Samplessample363
Known GenesIFNA13, IFNA2, IFNA6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088149
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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