A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569584



Internal ID16356993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57352069..57483608hg38UCSC Ensembl
Innerchr15:57644267..57775806hg19UCSC Ensembl
Innerchr15:55431559..55563098hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38131540
hg19131540
hg18131540
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4556n54
Supporting Variantsnssv843563, nssv843562
Samples
Known GenesCGNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569584
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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