A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570952



Internal ID16011675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:281959..286916hg38UCSC Ensembl
Innerchr16:331959..336916hg19UCSC Ensembl
Innerchr16:271960..276917hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384958
hg194958
hg184958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851305
Samples
Known GenesARHGDIG, PDIA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570952
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