A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059108



Internal ID19148327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580129..1591793hg38UCSC Ensembl
Innerchr20:1560775..1572439hg19UCSC Ensembl
Innerchr20:1508775..1520439hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3811665
hg1911665
hg1811665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4234n100
Supporting Variantsnssv3591557
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)nsv1059108
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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