A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555279



Internal ID15996002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68022085..68049469hg38UCSC Ensembl
Innerchr11:67789553..67816936hg19UCSC Ensembl
Innerchr11:67546129..67573512hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3827385
hg1927384
hg1827384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1983n54
Supporting Variantsnssv778612
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)nsv555279
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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