A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2824152



Internal ID15697530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:72075688..72078536hg38UCSC Ensembl
Innerchr16:72109587..72112435hg19UCSC Ensembl
Innerchr16:70667088..70669936hg18UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg382849
hg192849
hg182849
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514814
Supporting Variants
SamplesNA18870
Known GenesHPR
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2824152
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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