A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4242n100



Internal ID20155858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5464900..5825417hg38UCSC Ensembl
chr20:5445546..5806063hg19UCSC Ensembl
chr20:5393546..5754063hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38360518
hg19360518
hg18360518
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062448, nsv1058918
Samples
Known GenesC20orf196, GPCPD1, LINC00654, LOC643406
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4242n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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