A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556046



Internal ID15996769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99024489..99058829hg38UCSC Ensembl
Innerchr11:98895219..98929559hg19UCSC Ensembl
Innerchr11:98400429..98434769hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3834341
hg1934341
hg1834341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781719
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556046
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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