A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174799



Internal ID15529883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56736252..56936567hg38UCSC Ensembl
Innerchr11:56503728..56704042hg19UCSC Ensembl
Innerchr11:56260304..56460618hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38200316
hg19200315
hg18200315
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555101
Supporting Variants
SamplesHGDP00862
Known GenesMIR6128, OR9G4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174799
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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