A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065389



Internal ID19154608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580264..1617678hg38UCSC Ensembl
Innerchr20:1560910..1598324hg19UCSC Ensembl
Innerchr20:1508910..1546324hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3837415
hg1937415
hg1837415
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4233n100
Supporting Variantsnssv3595723, nssv3595721, nssv3595720, nssv3595725, nssv3595724, nssv3595719, nssv3595726, nssv3595722
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)nsv1065389
Frequency
Sample Size11257
Observed Gain6
Observed Loss2
Observed Complex0
Frequencyn/a


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