A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585240



Internal ID16372649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580578..1609342hg38UCSC Ensembl
Innerchr20:1561224..1589988hg19UCSC Ensembl
Innerchr20:1509224..1537988hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3828765
hg1928765
hg1828765
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7433n54
Supporting Variantsnssv936069
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585240
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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