A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7436n54



Internal ID22775331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1591228..1604232hg38UCSC Ensembl
chr20:1571874..1584878hg19UCSC Ensembl
chr20:1519874..1532878hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3813005
hg1913005
hg1813005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585254, nsv585253, nsv585251
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7436n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss115
Observed Complex0
Frequencyn/a


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