A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571292



Internal ID16358701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4315444..4316880hg38UCSC Ensembl
Innerchr16:4365445..4366881hg19UCSC Ensembl
Innerchr16:4305446..4306882hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381437
hg191437
hg181437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4883n54
Supporting Variantsnssv852328, nssv852327
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571292
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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