A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7432n54



Internal ID22775327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1577535..1591228hg38UCSC Ensembl
chr20:1558181..1571874hg19UCSC Ensembl
chr20:1506181..1519874hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3813694
hg1913694
hg1813694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585231, nsv585227, nsv585224, nsv585222, nsv585219
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7432n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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