A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566133



Internal ID16006856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104865282..104865448hg38UCSC Ensembl
Innerchr14:105331619..105331785hg19UCSC Ensembl
Innerchr14:104402664..104402830hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38167
hg19167
hg18167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834707
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566133
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