A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115368



Internal ID21298634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85383278..85386992hg38UCSC Ensembl
Innerchr9:87998193..88001907hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg383715
hg193715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088811
Samplessample385
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115368
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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