A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519408



Internal ID15100015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41559909..41667978hg38UCSC Ensembl
Innerchr19:42066279..42171906hg19UCSC Ensembl
Innerchr19:46758119..46863746hg18UCSC Ensembl
Innerchr19:46758119..46863746hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38108070
hg19105628
hg18105628
hg17105628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696837
Samples
Known GenesCEACAM21, CEACAM4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519408
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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