A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554044



Internal ID16341453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38230635..38304833hg38UCSC Ensembl
Innerchr11:38252185..38326383hg19UCSC Ensembl
Innerchr11:38208761..38282959hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3874199
hg1974199
hg1874199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1749n54
Supporting Variantsnssv771120, nssv771122, nssv771121, nssv771123
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554044
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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