A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599051



Internal ID18897332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580922..1618344hg38UCSC Ensembl
Innerchr20:1561568..1598990hg19UCSC Ensembl
Innerchr20:1509568..1546990hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3837423
hg1937423
hg1837423
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063396
Supporting Variants
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3599051
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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