A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585193



Internal ID16372602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:842861..942563hg38UCSC Ensembl
Innerchr20:823504..923206hg19UCSC Ensembl
Innerchr20:771504..871206hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3899703
hg1999703
hg1899703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv935341
Samples
Known GenesANGPT4, FAM110A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585193
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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