A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4280n100



Internal ID22790367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16583997..16615825hg38UCSC Ensembl
chr20:16564642..16596470hg19UCSC Ensembl
chr20:16512642..16544470hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3831829
hg1931829
hg1831829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057674, nsv1055217
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4280n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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