A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585191



Internal ID16025914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:680149..913482hg38UCSC Ensembl
Innerchr20:660793..894125hg19UCSC Ensembl
Innerchr20:608793..842125hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38233334
hg19233333
hg18233333
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv935339
Samples
Known GenesANGPT4, FAM110A, SLC52A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585191
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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