A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111986



Internal ID21295252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57686316..57693829hg38UCSC Ensembl
Innerchr16:57720228..57727741hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg387514
hg197514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv443n145
Supporting Variantsnssv14098292
Samplessample48
Known GenesGPR97
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111986
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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