A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554914



Internal ID15995637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55606497..55641188hg38UCSC Ensembl
Innerchr11:55373973..55408664hg19UCSC Ensembl
Innerchr11:55130549..55165240hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3834692
hg1934692
hg1834692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1911n54
Supporting Variantsnssv776526, nssv776527
Samples
Known GenesOR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554914
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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