A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059046



Internal ID19148265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580922..1618496hg38UCSC Ensembl
Innerchr20:1561568..1599142hg19UCSC Ensembl
Innerchr20:1509568..1547142hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3837575
hg1937575
hg1837575
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4233n100
Supporting Variantsnssv3599060, nssv3734673, nssv3599057, nssv3599055, nssv3599054, nssv3599056, nssv3599053, nssv3599061, nssv3599059, nssv3599058
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)nsv1059046
Frequency
Sample Size11257
Observed Gain8
Observed Loss2
Observed Complex0
Frequencyn/a


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