A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586029



Internal ID16026752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:43303515..43493820hg38UCSC Ensembl
Innerchr20:41932155..42122460hg19UCSC Ensembl
Innerchr20:41365569..41555874hg18UCSC Ensembl
Cytoband20q13.11
Allele length
AssemblyAllele length
hg38190306
hg19190306
hg18190306
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939507
Samples
Known GenesSRSF6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586029
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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