A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4286n100



Internal ID22790373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23694728..23769516hg38UCSC Ensembl
chr20:23675365..23750153hg19UCSC Ensembl
chr20:23623365..23698153hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3874789
hg1974789
hg1874789
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055248, nsv1059419
Samples
Known GenesCST1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4286n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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