A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751921



Internal ID20527781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24108999..24108999hg38UCSC Ensembl
chr16:24120320..24120320hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278864
Samples
Known GenesPRKCB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751921
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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