A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749345



Internal ID20525375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93768981..93769037hg38UCSC Ensembl
chr14:94235327..94235383hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285329
Samples
Known GenesPRIMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749345
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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