A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112768



Internal ID21296034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:151358895..151432320hg38UCSC Ensembl
Innerchr1:151331371..151404796hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3873426
hg1973426
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv76n145
Supporting Variantsnssv14095926
Samplessample318
Known GenesPOGZ, PSMB4, SELENBP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112768
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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