A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062597



Internal ID19151816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580922..1609797hg38UCSC Ensembl
Innerchr20:1561568..1590443hg19UCSC Ensembl
Innerchr20:1509568..1538443hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3828876
hg1928876
hg1828876
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4230n100
Supporting Variantsnssv3730940, nssv3730939
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)nsv1062597
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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