A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2786684



Internal ID15363966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62597244..62598188hg38UCSC Ensembl
Innerchr11:62364716..62365660hg19UCSC Ensembl
Innerchr11:62121292..62122236hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38945
hg19945
hg18945
Variant TypeCNV gain
Copy Number8
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514630
Supporting Variants
SamplesNA18956
Known GenesMTA2
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2786684
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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