A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112532



Internal ID21295798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13571254..13576094hg38UCSC Ensembl
Innerchr9:13571253..13576093hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg384841
hg194841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1220n145
Supporting Variantsnssv14088057
Samplessample314
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112532
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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