A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063396



Internal ID19152615
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4233n100
Supporting Variantsnssv3734672, nssv3599051
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)nsv1063396
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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