A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113953



Internal ID21297219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21719474..21721334hg38UCSC Ensembl
Innerchr9:21719473..21721333hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg381861
hg191861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088810
Samplessample385
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113953
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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