A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111068



Internal ID21294334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:59177204..59179750hg38UCSC Ensembl
Innerchr13:59751338..59753884hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg382547
hg192547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095836
Samplessample279
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111068
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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