A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14109208



Internal ID21278827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:19072487..19450514hg38UCSC Ensembl
Innerchr5:19072596..19450623hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38378028
hg19378028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115193
Supporting Variants
Samplessample274
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14109208
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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