A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585418



Internal ID16372827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:11665222..11667574hg38UCSC Ensembl
Innerchr20:11645870..11648222hg19UCSC Ensembl
Innerchr20:11593870..11596222hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg382353
hg192353
hg182353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937962
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585418
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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