A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063472



Internal ID19152691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1586796..1609876hg38UCSC Ensembl
Innerchr20:1567442..1590522hg19UCSC Ensembl
Innerchr20:1515442..1538522hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3823081
hg1923081
hg1823081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4236n100
Supporting Variantsnssv3599117, nssv3599118, nssv3599116
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)nsv1063472
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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