A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2785378



Internal ID15654774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5763645..5788012hg38UCSC Ensembl
Innerchr11:5784875..5809242hg19UCSC Ensembl
Innerchr11:5741451..5765818hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824368
hg1924368
hg1824368
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514624
Supporting Variants
SamplesNA12842
Known GenesOR52N1, OR52N5
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2785378
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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