A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv76n145



Internal ID22813092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151358895..151432320hg38UCSC Ensembl
chr1:151331371..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 Variants
Supporting Variantsnsv3112768, nsv3111469
Samplessample80, sample182, sample170, sample91, sample383, sample375, sample56, sample287, sample43, sample318, sample246, sample268, sample163
Known GenesPOGZ, PSMB4, SELENBP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv76n145
Frequency
Sample Size467
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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