A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593756



Internal ID16034479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:14896504..14935342hg38UCSC Ensembl
Innerchr4:14898128..14936966hg19UCSC Ensembl
Innerchr4:14507226..14546064hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3838839
hg1938839
hg1838839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv993081
Samples
Known GenesCPEB2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593756
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