A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv936587



Internal ID16230543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1586749..1611843hg38UCSC Ensembl
Innerchr20:1567395..1592489hg19UCSC Ensembl
Innerchr20:1515395..1540489hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3825095
hg1925095
hg1825095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585247
Supporting Variants
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv936587
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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