A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585237



Internal ID16372646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580316..1613627hg38UCSC Ensembl
Innerchr20:1560962..1594273hg19UCSC Ensembl
Innerchr20:1508962..1542273hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3833312
hg1933312
hg1833312
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7433n54
Supporting Variantsnssv936064, nssv936063, nssv936062
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585237
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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