A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2787608



Internal ID15346609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107368400..107372016hg38UCSC Ensembl
Innerchr11:107239126..107242742hg19UCSC Ensembl
Innerchr11:106744336..106747952hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg383617
hg193617
hg183617
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514590
Supporting Variants
SamplesNA18857
Known GenesCWF19L2
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2787608
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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