A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4236n100



Internal ID22790323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1586796..1613191hg38UCSC Ensembl
chr20:1567442..1593837hg19UCSC Ensembl
chr20:1515442..1541837hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3826396
hg1926396
hg1826396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058582, nsv1067271, nsv1062630, nsv1061362, nsv1060173, nsv1062795, nsv1067018, nsv1067061, nsv1057515, nsv1059713, nsv1059452, nsv1063472, nsv1062091, nsv1060230, nsv1066749, nsv1060841, nsv1058369, nsv1061479, nsv1059032, nsv1059590, nsv1060943, nsv1067371, nsv1060102
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)dgv4236n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss201
Observed Complex0
Frequencyn/a


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