A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570950



Internal ID16011673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:279671..286396hg38UCSC Ensembl
Innerchr16:329671..336396hg19UCSC Ensembl
Innerchr16:269672..276397hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386726
hg196726
hg186726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4808n54
Supporting Variantsnssv851303
Samples
Known GenesARHGDIG, PDIA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570950
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