A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552867



Internal ID16340276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:647869..688312hg38UCSC Ensembl
Innerchr11:647869..688312hg19UCSC Ensembl
Innerchr11:637869..678312hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3840444
hg1940444
hg1840444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1525n54
Supporting Variantsnssv763562
Samples
Known GenesDEAF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552867
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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