A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554039



Internal ID16341448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38227656..38363288hg38UCSC Ensembl
Innerchr11:38249206..38384838hg19UCSC Ensembl
Innerchr11:38205782..38341414hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38135633
hg19135633
hg18135633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1751n54
Supporting Variantsnssv771108
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554039
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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