A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114172



Internal ID21297438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31007179..31009219hg38UCSC Ensembl
Innerchr13:31581316..31583356hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg382041
hg192041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093003
Samplessample424
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114172
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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