A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057701



Internal ID19146920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580341..1609876hg38UCSC Ensembl
Innerchr20:1560987..1590522hg19UCSC Ensembl
Innerchr20:1508987..1538522hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3829536
hg1929536
hg1829536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4230n100
Supporting Variantsnssv3595915, nssv3595916, nssv3595918, nssv3595919, nssv3728592, nssv3595920, nssv3595917
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)nsv1057701
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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