A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090816



Internal ID21273161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:106869121..106878040hg38UCSC Ensembl
Innerchr9:109631402..109640321hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg388920
hg198920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111853
Supporting Variants
Samplessample188
Known GenesZNF462
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090816
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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