A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565863



Internal ID16353272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101452879..101459545hg38UCSC Ensembl
Innerchr14:101919216..101925882hg19UCSC Ensembl
Innerchr14:100988969..100995635hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg386667
hg196667
hg186667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833681
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565863
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