A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585416



Internal ID16372825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:11176127..11209439hg38UCSC Ensembl
Innerchr20:11156775..11190087hg19UCSC Ensembl
Innerchr20:11104775..11138087hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3833313
hg1933313
hg1833313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937961
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585416
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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