A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919278



Internal ID22694500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11015328..11070477hg38UCSC Ensembl
chr12:11167927..11223076hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3855150
hg1955150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv339n209
Supporting Variantsnssv17353265
Samples
Known GenesPRH1-PRR4, TAS2R19, TAS2R31, TAS2R46
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919278
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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