A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555456



Internal ID16342865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:79153560..79171127hg38UCSC Ensembl
Innerchr11:78864605..78882172hg19UCSC Ensembl
Innerchr11:78542253..78559820hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3817568
hg1917568
hg1817568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv779227
Samples
Known GenesTENM4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555456
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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