A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063495



Internal ID18806026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:38295280..38457885hg38UCSC Ensembl
Innerchr20:36923682..37086528hg19UCSC Ensembl
Innerchr20:36357096..36519942hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38162606
hg19162847
hg18162847
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584775
Samples
Known GenesBPI, LBP, SNHG11, SNHG17, SNORA39, SNORA60, SNORA71A, SNORA71B, SNORA71C, SNORA71D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063495
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer