A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4284n100



Internal ID22790371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19089508..19117867hg38UCSC Ensembl
chr20:19070152..19098511hg19UCSC Ensembl
chr20:19018152..19046511hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3828360
hg1928360
hg1828360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056167, nsv1064120
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)dgv4284n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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