A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585238



Internal ID16372647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580578..1600450hg38UCSC Ensembl
Innerchr20:1561224..1581096hg19UCSC Ensembl
Innerchr20:1509224..1529096hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3819873
hg1919873
hg1819873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv936065
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585238
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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