A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020666



Internal ID19109885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18824078..18949411hg38UCSC Ensembl
Innerchr5:18824187..18949520hg19UCSC Ensembl
Innerchr5:18859944..18985277hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38125334
hg19125334
hg18125334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5595n100
Supporting Variantsnssv3635897, nssv3635898
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)nsv1020666
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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