A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586134



Internal ID16026857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45899835..45905120hg38UCSC Ensembl
Innerchr20:44528474..44533759hg19UCSC Ensembl
Innerchr20:43961881..43967166hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg385286
hg195286
hg185286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv940871
Samples
Known GenesPLTP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586134
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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