A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571493



Internal ID16012216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13200856..13206350hg38UCSC Ensembl
Innerchr16:13294713..13300207hg19UCSC Ensembl
Innerchr16:13202214..13207708hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg385495
hg195495
hg185495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4914n54
Supporting Variantsnssv852742
Samples
Known GenesSHISA9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571493
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