A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4223n100



Internal ID22790310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1566104..1617288hg38UCSC Ensembl
chr20:1546750..1597934hg19UCSC Ensembl
chr20:1494750..1545934hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3851185
hg1951185
hg1851185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055446, nsv1060586, nsv1063461
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)dgv4223n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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