A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585359



Internal ID16372768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7409935..7419548hg38UCSC Ensembl
Innerchr20:7390582..7400195hg19UCSC Ensembl
Innerchr20:7338582..7348195hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg389614
hg199614
hg189614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937579
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585359
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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