A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834680



Internal ID15781950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104865033..104865725hg38UCSC Ensembl
Innerchr14:105331370..105332062hg19UCSC Ensembl
Innerchr14:104402415..104403107hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38693
hg19693
hg18693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566119
Supporting Variants
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834680
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