A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552762



Internal ID16340171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:198510..274780hg38UCSC Ensembl
Innerchr11:198510..274780hg19UCSC Ensembl
Innerchr11:188510..264780hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3876271
hg1976271
hg1876271
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175074
SamplesHGDP01371
Known GenesBET1L, MIR6743, ODF3, PSMD13, RIC8A, SIRT3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552762
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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