A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571159



Internal ID16011882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1373157..1376586hg38UCSC Ensembl
Innerchr16:1423158..1426587hg19UCSC Ensembl
Innerchr16:1363159..1366588hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383430
hg193430
hg183430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4853n54
Supporting Variantsnssv852054
Samples
Known GenesUNKL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571159
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