A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571257



Internal ID16011980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3655014..3668847hg38UCSC Ensembl
Innerchr16:3705015..3718848hg19UCSC Ensembl
Innerchr16:3645016..3658849hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3813834
hg1913834
hg1813834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4876n54
Supporting Variantsnssv852265, nssv1148909
SamplesHGDP01066
Known GenesDNASE1, TRAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571257
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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