A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603088



Internal ID16390497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:49463856..49478791hg38UCSC Ensembl
Innerchr6:49431569..49446504hg19UCSC Ensembl
Innerchr6:49539528..49554463hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3814936
hg1914936
hg1814936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10655n54
Supporting Variantsnssv1058825
Samples
Known GenesCENPQ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603088
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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