A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565031



Internal ID16352440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70221751..70222487hg38UCSC Ensembl
Innerchr14:70688468..70689204hg19UCSC Ensembl
Innerchr14:69758221..69758957hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38737
hg19737
hg18737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3750n54
Supporting Variantsnssv829049, nssv829048
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565031
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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