A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585428



Internal ID16372837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:12254154..12383615hg38UCSC Ensembl
Innerchr20:12234802..12364263hg19UCSC Ensembl
Innerchr20:12182802..12312263hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38129462
hg19129462
hg18129462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938029
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585428
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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