A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057680



Internal ID19146899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580264..1617288hg38UCSC Ensembl
Innerchr20:1560910..1597934hg19UCSC Ensembl
Innerchr20:1508910..1545934hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3837025
hg1937025
hg1837025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4230n100
Supporting Variantsnssv3595715, nssv3595713, nssv3595714, nssv3595717, nssv3595716, nssv3595712, nssv3595710, nssv3595711, nssv3728552, nssv3595709
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)nsv1057680
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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