A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4233n100



Internal ID22790320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1579885..1618496hg38UCSC Ensembl
chr20:1560531..1599142hg19UCSC Ensembl
chr20:1508531..1547142hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3838612
hg1938612
hg1838612
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066711, nsv1056547, nsv1056403, nsv1064704, nsv1058817, nsv1057641, nsv1060078, nsv1062208, nsv1060856, nsv1064586, nsv1055362, nsv1061770, nsv1064634, nsv1065389, nsv1063396, nsv1065781, nsv1058246, nsv1058381, nsv1056838, nsv1063406, nsv1059046, nsv1058095
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4233n100
Frequency
Sample Size11257
Observed Gain3156
Observed Loss636
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer