A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571465



Internal ID16358874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12531538..12545943hg38UCSC Ensembl
Innerchr16:12625395..12639800hg19UCSC Ensembl
Innerchr16:12532896..12547301hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3814406
hg1914406
hg1814406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852538
Samples
Known GenesSNX29
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571465
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