A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695691



Internal ID15432343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27931350..27951885hg38UCSC Ensembl
Innerchr14:28400556..28421091hg19UCSC Ensembl
Innerchr14:27470396..27490931hg18UCSC Ensembl
Innerchr14:27470396..27490931hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3820536
hg1920536
hg1820536
hg1720536
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518260
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695691
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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