A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554035



Internal ID16341444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38227656..38304833hg38UCSC Ensembl
Innerchr11:38249206..38326383hg19UCSC Ensembl
Innerchr11:38205782..38282959hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3877178
hg1977178
hg1877178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1749n54
Supporting Variantsnssv771103
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554035
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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