A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585188



Internal ID16025911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:641912..650781hg38UCSC Ensembl
Innerchr20:622556..631425hg19UCSC Ensembl
Innerchr20:570556..579425hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg388870
hg198870
hg188870
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv935325
Samples
Known GenesSRXN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585188
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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