A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2821545



Internal ID15334327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70114836..70162524hg38UCSC Ensembl
Innerchr16:70148739..70196427hg19UCSC Ensembl
Innerchr16:68706240..68753928hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3847689
hg1947689
hg1847689
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514810
Supporting Variants
SamplesNA18576
Known GenesPDPR
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2821545
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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