A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112281



Internal ID21295547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102393450..102499334hg38UCSC Ensembl
Innerchr9:105155732..105261616hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38105885
hg19105885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088894
Samplessample423
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112281
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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