A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112946



Internal ID21296212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:82315540..82318278hg38UCSC Ensembl
Innerchr9:84930455..84933193hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg382739
hg192739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1240n145
Supporting Variantsnssv14090868
Samplessample216
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112946
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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