A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553235



Internal ID16340644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5361785..5362357hg38UCSC Ensembl
Innerchr11:5383015..5383587hg19UCSC Ensembl
Innerchr11:5339591..5340163hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38573
hg19573
hg18573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv765359
Samples
Known GenesOR51B5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553235
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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