A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096809



Internal ID21289251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151410985..151419218hg38UCSC Ensembl
Innerchr5:150790546..150798779hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg388234
hg198234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115564
Supporting Variants
Samplessample45
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096809
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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