A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117299



Internal ID21300565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23290596..23297798hg38UCSC Ensembl
Innerchr9:23290594..23297796hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg387203
hg197203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1225n145
Supporting Variantsnssv14089557, nssv14088393, nssv14089539, nssv14089585, nssv14088038, nssv14087927
Samplessample90, sample78, sample71, sample304, sample1, sample259
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117299
Frequency
Sample Size467
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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