A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060019



Internal ID19149238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580144..1617288hg38UCSC Ensembl
Innerchr20:1560790..1597934hg19UCSC Ensembl
Innerchr20:1508790..1545934hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3837145
hg1937145
hg1837145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4230n100
Supporting Variantsnssv3594385, nssv3594384
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)nsv1060019
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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