A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096538



Internal ID21283629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81314754..81317293hg38UCSC Ensembl
Innerchr16:81348359..81350898hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg382540
hg192540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116861
Supporting Variants
Samplessample348
Known GenesGAN
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096538
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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