A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098268



Internal ID21285822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:59802825..59808197hg38UCSC Ensembl
Innerchr16:59836729..59842101hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385373
hg195373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117621
Supporting Variants
Samplessample38
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098268
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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