A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111721



Internal ID21294987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23289386..23296952hg38UCSC Ensembl
Innerchr9:23289384..23296950hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg387567
hg197567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1225n145
Supporting Variantsnssv14089464, nssv14086902
Samplessample222, sample41
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111721
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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