A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116230



Internal ID21299496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5861879..5866364hg38UCSC Ensembl
Innerchr9:5861879..5866364hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg384486
hg194486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088430
Samplessample19
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116230
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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