A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4301n100



Internal ID20155917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33026982..33050770hg38UCSC Ensembl
chr20:31614788..31638576hg19UCSC Ensembl
chr20:31078449..31102237hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3823789
hg1923789
hg1823789
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1067509, nsv1058726
Samples
Known GenesBPIFB6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4301n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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