A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585720



Internal ID16373129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:22352470..22395783hg38UCSC Ensembl
Innerchr20:22333108..22376421hg19UCSC Ensembl
Innerchr20:22281108..22324421hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3843314
hg1943314
hg1843314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938916
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585720
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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