A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864226



Internal ID22639161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106440069..106442324hg38UCSC Ensembl
chr12:106833847..106836102hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg382256
hg192256
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459514
Samples
Known GenesPOLR3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864226
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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