A curated catalogue of human genomic structural variation




Variant Details

Variant: esv991867



Internal ID7077541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580305..1613247hg38UCSC Ensembl
Innerchr20:1560951..1593893hg19UCSC Ensembl
Innerchr20:1508951..1541893hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3832943
hg1932943
hg1832943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586018
SamplesHuRef
Known GenesSIRPB1
MethodSNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv991867
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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