A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117283



Internal ID21300549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97096486..97127615hg38UCSC Ensembl
Innerchr9:99858768..99889897hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3831130
hg1931130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089746
Samplessample157
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117283
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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