A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111806



Internal ID21295072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7212624..7228168hg38UCSC Ensembl
Innerchr9:7212624..7228168hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3815545
hg1915545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089683
Samplessample133
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111806
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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