A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060775



Internal ID19149994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32197413..33656142hg38UCSC Ensembl
Innerchr16:32208734..33458609hg19UCSC Ensembl
Innerchr16:32116235..33366110hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381458730
hg191249876
hg181249876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2842n100
Supporting Variantsnssv3550402
Samples
Known GenesLOC390705, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060775
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