A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585248



Internal ID16372657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1586749..1613627hg38UCSC Ensembl
Innerchr20:1567395..1594273hg19UCSC Ensembl
Innerchr20:1515395..1542273hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3826879
hg1926879
hg1826879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7434n54
Supporting Variantsnssv936632
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585248
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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