A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554074



Internal ID16341483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38970996..39053004hg38UCSC Ensembl
Innerchr11:38992546..39074554hg19UCSC Ensembl
Innerchr11:38949122..39031130hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3882009
hg1982009
hg1882009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv771154
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554074
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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