A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116370



Internal ID21299636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81314754..81317497hg38UCSC Ensembl
Innerchr16:81348359..81351102hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg382744
hg192744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv468n145
Supporting Variantsnssv14096542
Samplessample349
Known GenesGAN
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116370
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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