A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095836



Internal ID21279195
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 StatusS
Merged Variantsnsv3111068
Supporting Variants
Samplessample279
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095836
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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