A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553776



Internal ID16341185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23988984..24064194hg38UCSC Ensembl
Innerchr11:24010530..24085740hg19UCSC Ensembl
Innerchr11:23967106..24042316hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3875211
hg1975211
hg1875211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1698n54
Supporting Variantsnssv1174755
Samples1780862432_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553776
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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