A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578128



Internal ID16365537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:539266..540727hg38UCSC Ensembl
Innerchr19:539266..540727hg19UCSC Ensembl
Innerchr19:490266..491727hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381462
hg191462
hg181462
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891143
Samples
Known GenesCDC34
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578128
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