A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585254



Internal ID16372663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1591728..1604232hg38UCSC Ensembl
Innerchr20:1572374..1584878hg19UCSC Ensembl
Innerchr20:1520374..1532878hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3812505
hg1912505
hg1812505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7436n54
Supporting Variantsnssv936939
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585254
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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