A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579327



Internal ID16020050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33620377..33622206hg38UCSC Ensembl
Innerchr19:34111283..34113112hg19UCSC Ensembl
Innerchr19:38803123..38804952hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381830
hg191830
hg181830
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6404n54
Supporting Variantsnssv898497
Samples
Known GenesCHST8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579327
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