A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585352



Internal ID16372761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:6148621..6149930hg38UCSC Ensembl
Innerchr20:6129268..6130577hg19UCSC Ensembl
Innerchr20:6077268..6078577hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg381310
hg191310
hg181310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937572
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585352
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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