A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059686



Internal ID19148905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:60990189..61015439hg38UCSC Ensembl
Innerchr20:59565245..59590495hg19UCSC Ensembl
Innerchr20:58998640..59023890hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3825251
hg1925251
hg1825251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4340n100
Supporting Variantsnssv3584350
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059686
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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