A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094352



Internal ID21279865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73392577..73412693hg38UCSC Ensembl
Innerchr13:73966714..73986830hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3820117
hg1920117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111113
Supporting Variants
Samplessample29
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094352
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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