A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2622n100



Internal ID20154238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75904333..76022201hg38UCSC Ensembl
chr15:76196674..76314542hg19UCSC Ensembl
chr15:73983729..74101597hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38117869
hg19117869
hg18117869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040053, nsv1053717
Samples
Known GenesFBXO22, FBXO22-AS1, NRG4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2622n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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