A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585217



Internal ID16372626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1577098..1601742hg38UCSC Ensembl
Innerchr20:1557744..1582388hg19UCSC Ensembl
Innerchr20:1505744..1530388hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3824645
hg1924645
hg1824645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7431n54
Supporting Variantsnssv935911, nssv935909, nssv935917, nssv935910, nssv935915, nssv935912, nssv935922, nssv935916, nssv935913, nssv935921, nssv935919, nssv935920, nssv935914, nssv935918, nssv935908
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585217
Frequency
Sample Size17421
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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