A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016168



Internal ID19105386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152132075..152142822hg38UCSC Ensembl
Innerchr5:151511636..151522383hg19UCSC Ensembl
Innerchr5:151491829..151502576hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3810748
hg1910748
hg1810748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5819n100
Supporting Variantsnssv3648180
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)nsv1016168
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