A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116011



Internal ID21299277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13809779..13821054hg38UCSC Ensembl
Innerchr9:13809778..13821053hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3811276
hg1911276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087960
Samplessample271
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116011
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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