A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090334



Internal ID21287271
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 StatusS
Merged Variantsnsv3116010
Supporting Variants
Samplessample4
Known GenesPRH1-PRR4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090334
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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