A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113893



Internal ID21297159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20794562..20804552hg38UCSC Ensembl
Innerchr9:20794561..20804551hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg389991
hg199991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1223n145
Supporting Variantsnssv14090820, nssv14088091
Samplessample328, sample190
Known GenesFOCAD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113893
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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