A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016135



Internal ID19105353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18305915..18330830hg38UCSC Ensembl
Innerchr5:18306024..18330939hg19UCSC Ensembl
Innerchr5:18341781..18366696hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3824916
hg1924916
hg1824916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635856
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016135
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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