A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571832



Internal ID16359241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32153014..32586373hg38UCSC Ensembl
Innerchr16:32164335..32597694hg19UCSC Ensembl
Innerchr16:32071836..32505195hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38433360
hg19433360
hg18433360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4991n54
Supporting Variantsnssv855511
Samples
Known GenesLOC390705, TP53TG3D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571832
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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