A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586236



Internal ID16026959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54030387..54041462hg38UCSC Ensembl
Innerchr20:52646926..52658001hg19UCSC Ensembl
Innerchr20:52080333..52091408hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3811076
hg1911076
hg1811076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7608n54
Supporting Variantsnssv941244, nssv941246, nssv941247, nssv941245
Samples
Known GenesBCAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586236
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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