A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113222



Internal ID21296488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119137306..119148783hg38UCSC Ensembl
Innerchr8:120149545..120161022hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3811478
hg1911478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087244
Samplessample279
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113222
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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