A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562146



Internal ID16349555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68301056..68464322hg38UCSC Ensembl
Innerchr13:68875188..69038454hg19UCSC Ensembl
Innerchr13:67773189..67936455hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38163267
hg19163267
hg18163267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813417
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562146
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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