A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116010



Internal ID21299276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10963629..10973479hg38UCSC Ensembl
Innerchr12:11116228..11126078hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg389851
hg199851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092574, nssv14090334
Samplessample4, sample292
Known GenesPRH1-PRR4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116010
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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