A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2835366



Internal ID15675514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14477548..14594526hg38UCSC Ensembl
Innerchr18:14477547..14594525hg19UCSC Ensembl
Innerchr18:14467547..14584525hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38116979
hg19116979
hg18116979
Variant TypeCNV gain
Copy Number9
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514861
Supporting Variants
SamplesNA18550
Known GenesCXADRP3, POTEC
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2835366
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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