A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3715n100



Internal ID20155331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10014833..10135998hg38UCSC Ensembl
chr2:10154960..10276125hg19UCSC Ensembl
chr2:10072411..10193576hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38121166
hg19121166
hg18121166
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999019, nsv1007965
Samples
Known GenesCYS1, KLF11, RRM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3715n100
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