A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2863507



Internal ID15799974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1582985..1603285hg38UCSC Ensembl
Innerchr20:1563631..1583931hg19UCSC Ensembl
Innerchr20:1511631..1531931hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3820301
hg1920301
hg1820301
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514932
Supporting Variants
SamplesNA21490
Known GenesSIRPB1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2863507
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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