A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556387



Internal ID16343796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107785223..107800900hg38UCSC Ensembl
Innerchr11:107655949..107671626hg19UCSC Ensembl
Innerchr11:107161159..107176836hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3815678
hg1915678
hg1815678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2176n54
Supporting Variantsnssv784255, nssv784230, nssv784244, nssv784265, nssv784241, nssv784239, nssv784261, nssv784251, nssv784242, nssv784259, nssv784262, nssv784267, nssv784258, nssv784232, nssv784256, nssv784246, nssv784254, nssv784236, nssv784249, nssv784235, nssv784231, nssv784252, nssv784253, nssv784238, nssv784247, nssv784263, nssv784233, nssv784260, nssv784245, nssv784248, nssv784268, nssv784257, nssv784234, nssv784237, nssv784243, nssv784266, nssv784264, nssv784250, nssv784240
Samples
Known GenesSLC35F2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556387
Frequency
Sample Size17421
Observed Gain39
Observed Loss0
Observed Complex0
Frequencyn/a


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