A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556110



Internal ID16343519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99722154..99765452hg38UCSC Ensembl
Innerchr11:99592885..99636183hg19UCSC Ensembl
Innerchr11:99098095..99141393hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3843299
hg1943299
hg1843299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2129n54
Supporting Variantsnssv781982
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556110
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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