A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2864064



Internal ID15759106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:451158..452288hg38UCSC Ensembl
Innerchr1:367049..368179hg19UCSC Ensembl
Innerchr1:356912..358042hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg381131
hg191131
hg181131
Variant TypeCNV gain
Copy Number15
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514924
Supporting Variants
SamplesNA19197
Known GenesOR4F16, OR4F29, OR4F3
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2864064
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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