A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941245



Internal ID15888515
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 StatusS
Merged Variantsnsv586236
Supporting Variants
Samples
Known GenesBCAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv941245
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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