A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089903



Internal ID21278393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:151360968..151432320hg38UCSC Ensembl
Innerchr1:151333444..151404796hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3871353
hg1971353
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111469
Supporting Variants
Samplessample268
Known GenesPOGZ, PSMB4, SELENBP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089903
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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