A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7714n100



Internal ID20159330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122107328..122135503hg38UCSC Ensembl
chr9:124869607..124897782hg19UCSC Ensembl
chr9:123909428..123937603hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3828176
hg1928176
hg1828176
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045766, nsv1038490
Samples
Known GenesMIR4478
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7714n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer