A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554042



Internal ID16341451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38230635..38294034hg38UCSC Ensembl
Innerchr11:38252185..38315584hg19UCSC Ensembl
Innerchr11:38208761..38272160hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3863400
hg1963400
hg1863400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1749n54
Supporting Variantsnssv771110, nssv771112, nssv771111, nssv771113, nssv771114
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554042
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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