A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585866



Internal ID16373275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:30190681..30323787hg38UCSC Ensembl
Innerchr20:29425357..29558463hg19UCSC Ensembl
Innerchr20:28039018..28172124hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg38133107
hg19133107
hg18133107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939187
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585866
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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