A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv160n100



Internal ID20151776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46805270..46856310hg38UCSC Ensembl
chr1:47270942..47321982hg19UCSC Ensembl
chr1:47043529..47094569hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3851041
hg1951041
hg1851041
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004246, nsv1004143
Samples
Known GenesCYP4B1, CYP4Z2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv160n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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