A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110941



Internal ID21294207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14312143..14313672hg38UCSC Ensembl
Innerchr9:14312142..14313671hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg381530
hg191530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088124
Samplessample348
Known GenesNFIB
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110941
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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