A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554027



Internal ID16341436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38109249..38318734hg38UCSC Ensembl
Innerchr11:38130799..38340284hg19UCSC Ensembl
Innerchr11:38087375..38296860hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38209486
hg19209486
hg18209486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1748n54
Supporting Variantsnssv771084
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554027
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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