A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096411



Internal ID21278776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58933968..58940838hg38UCSC Ensembl
Innerchr16:58967872..58974742hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg386871
hg196871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116882
Supporting Variants
Samplessample273
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096411
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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