A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099205



Internal ID21272798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65142617..65143315hg38UCSC Ensembl
Innerchr16:65176520..65177218hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110752
Supporting Variants
Samplessample182
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099205
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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