A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5811n54



Internal ID22773706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:841320..1798153hg38UCSC Ensembl
chr18:841321..1798154hg19UCSC Ensembl
chr18:831321..1788154hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38956834
hg19956834
hg18956834
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576247, nsv576246, nsv576248
Samples
Known GenesADCYAP1, LINC00470
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5811n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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