A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553451



Internal ID15994174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8937473..8941217hg38UCSC Ensembl
Innerchr11:8959020..8962764hg19UCSC Ensembl
Innerchr11:8915596..8919340hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383745
hg193745
hg183745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv767055
Samples
Known GenesASCL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553451
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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