A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114525



Internal ID21297791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85286183..85291851hg38UCSC Ensembl
Innerchr9:87901098..87906766hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg385669
hg195669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1241n145
Supporting Variantsnssv14089545
Samplessample73
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114525
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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