A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553449



Internal ID16340858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8937356..8943144hg38UCSC Ensembl
Innerchr11:8958903..8964691hg19UCSC Ensembl
Innerchr11:8915479..8921267hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385789
hg195789
hg185789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1640n54
Supporting Variantsnssv767052
Samples
Known GenesASCL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553449
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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