A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555280



Internal ID15996003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68025546..68049469hg38UCSC Ensembl
Innerchr11:67793014..67816936hg19UCSC Ensembl
Innerchr11:67549590..67573512hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3823924
hg1923923
hg1823923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1983n54
Supporting Variantsnssv778613
Samples
Known GenesALDH3B1, MIR4691, MIR6753, MIR7113, NDUFS8, TCIRG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555280
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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