A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067282



Internal ID19156501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:60891862..61013529hg38UCSC Ensembl
Innerchr20:59466918..59588585hg19UCSC Ensembl
Innerchr20:58900313..59021980hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38121668
hg19121668
hg18121668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4338n100
Supporting Variantsnssv3584324
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)nsv1067282
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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