A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585331



Internal ID16372740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5720835..5838899hg38UCSC Ensembl
Innerchr20:5701481..5819545hg19UCSC Ensembl
Innerchr20:5649481..5767545hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38118065
hg19118065
hg18118065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937459
Samples
Known GenesC20orf196
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585331
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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