A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554023



Internal ID16341432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38071118..38300656hg38UCSC Ensembl
Innerchr11:38092668..38322206hg19UCSC Ensembl
Innerchr11:38049244..38278782hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38229539
hg19229539
hg18229539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1748n54
Supporting Variantsnssv771080, nssv771079, nssv771081
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554023
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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