A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060201



Internal ID19149420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:706472..739210hg38UCSC Ensembl
Innerchr20:687116..719854hg19UCSC Ensembl
Innerchr20:635116..667854hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3832739
hg1932739
hg1832739
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589962
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)nsv1060201
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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