A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890277



Internal ID167681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151359589..151436025hg38UCSC Ensembl
chr1:151332065..151408501hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3876437
hg1976437
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138677
Supporting Variants
Samples
Known GenesPOGZ, PSMB4, SELENBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890277
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002655


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