A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585205



Internal ID16372614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1259541..1260223hg38UCSC Ensembl
Innerchr20:1240185..1240867hg19UCSC Ensembl
Innerchr20:1188185..1188867hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38683
hg19683
hg18683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv935356
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585205
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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