A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089695



Internal ID21269325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121022899..121025864hg38UCSC Ensembl
Innerchr9:123785177..123788142hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg382966
hg192966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118350
Supporting Variants
Samplessample138
Known GenesC5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089695
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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