A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555282



Internal ID15996005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68031100..68050858hg38UCSC Ensembl
Innerchr11:67798567..67818325hg19UCSC Ensembl
Innerchr11:67555143..67574901hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3819759
hg1919759
hg1819759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv778615
Samples
Known GenesMIR4691, MIR6753, MIR7113, NDUFS8, TCIRG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555282
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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