A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098208



Internal ID21287253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:52906994..52915449hg38UCSC Ensembl
Innerchr16:52940906..52949361hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg388456
hg198456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117185
Supporting Variants
Samplessample4
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098208
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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