A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564158



Internal ID16351567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28728853..28738995hg38UCSC Ensembl
Innerchr14:29198059..29208201hg19UCSC Ensembl
Innerchr14:28267810..28277952hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3810143
hg1910143
hg1810143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3603n54
Supporting Variantsnssv825108
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564158
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