A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4224n100



Internal ID22790311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1571458..1591793hg38UCSC Ensembl
chr20:1552104..1572439hg19UCSC Ensembl
chr20:1500104..1520439hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3820336
hg1920336
hg1820336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062968, nsv1055518, nsv1061826, nsv1066494
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)dgv4224n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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