A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4293n100



Internal ID22790380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:26229106..26324931hg38UCSC Ensembl
chr20:26209742..26305567hg19UCSC Ensembl
chr20:26157742..26253567hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3895826
hg1995826
hg1895826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056353, nsv1062036, nsv1067296, nsv1061873, nsv1062374, nsv1064464
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)dgv4293n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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