A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082559



Internal ID21284807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5299557..5306121hg38UCSC Ensembl
Innerchr5:5299670..5306234hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg386565
hg196565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115335
Supporting Variants
Samplessample365
Known GenesADAMTS16
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082559
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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