A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981509



Internal ID21890852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151359872..151436237hg38UCSC Ensembl
chr1:151332348..151408713hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3876366
hg1976366
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520335
Samples
Known GenesPOGZ, PSMB4, SELENBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981509
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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