A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4294n100



Internal ID22790381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30185664..30271217hg38UCSC Ensembl
chr20:29420340..29505893hg19UCSC Ensembl
chr20:28034001..28119554hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg3885554
hg1985554
hg1885554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061076, nsv1056639
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)dgv4294n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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