A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571059



Internal ID16358468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:966057..997729hg38UCSC Ensembl
Innerchr16:1016057..1047729hg19UCSC Ensembl
Innerchr16:956058..987730hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3831673
hg1931673
hg1831673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149284
SamplesHGDP01271
Known GenesLMF1, SOX8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571059
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