A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572926



Internal ID16013649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70153367..70162848hg38UCSC Ensembl
Innerchr16:70187270..70196751hg19UCSC Ensembl
Innerchr16:68744771..68754252hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg389482
hg199482
hg189482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5180n54
Supporting Variantsnssv859094
Samples
Known GenesPDPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572926
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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