A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586206



Internal ID16373615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:52265812..52303502hg38UCSC Ensembl
Innerchr20:50882351..50920041hg19UCSC Ensembl
Innerchr20:50315758..50353448hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3837691
hg1937691
hg1837691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941150
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586206
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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