A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570951



Internal ID16011674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:279671..322597hg38UCSC Ensembl
Innerchr16:329671..372597hg19UCSC Ensembl
Innerchr16:269672..312598hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3842927
hg1942927
hg1842927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851304
Samples
Known GenesARHGDIG, AXIN1, PDIA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570951
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