A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089746



Internal ID21270998
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 StatusS
Merged Variantsnsv3117283
Supporting Variants
Samplessample157
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089746
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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