A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554021



Internal ID16341430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37923359..37970271hg38UCSC Ensembl
Innerchr11:37944909..37991821hg19UCSC Ensembl
Innerchr11:37901485..37948397hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3846913
hg1946913
hg1846913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1747n54
Supporting Variantsnssv771078
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554021
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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