A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7434n54



Internal ID22775329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1583892..1613627hg38UCSC Ensembl
chr20:1564538..1594273hg19UCSC Ensembl
chr20:1512538..1542273hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3829736
hg1929736
hg1829736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585247, nsv585255, nsv585250, nsv585248, nsv585252, nsv585245
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7434n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss850
Observed Complex0
Frequencyn/a


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