A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113236



Internal ID21296502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:90886472..90887637hg38UCSC Ensembl
Innerchr13:91538726..91539891hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv309n145
Supporting Variantsnssv14094452, nssv14095859, nssv14096958
Samplessample361, sample79, sample292
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113236
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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