A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111853



Internal ID21295119
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 StatusM
Merged Variants
Supporting Variantsnssv14090816
Samplessample188
Known GenesZNF462
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111853
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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