A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553450



Internal ID16340859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8937356..8943391hg38UCSC Ensembl
Innerchr11:8958903..8964938hg19UCSC Ensembl
Innerchr11:8915479..8921514hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg386036
hg196036
hg186036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1640n54
Supporting Variantsnssv767054, nssv767053
Samples
Known GenesASCL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553450
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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