A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108881



Internal ID21272741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178777482..178792943hg38UCSC Ensembl
Innerchr5:178204483..178219944hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3815462
hg1915462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115185
Supporting Variants
Samplessample181
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108881
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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