A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554079



Internal ID16341488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:39057598..39110310hg38UCSC Ensembl
Innerchr11:39079148..39131860hg19UCSC Ensembl
Innerchr11:39035724..39088436hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3852713
hg1952713
hg1852713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1757n54
Supporting Variantsnssv771163, nssv771162
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554079
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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