A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556280



Internal ID16343689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107288014..107360879hg38UCSC Ensembl
Innerchr11:107158740..107231605hg19UCSC Ensembl
Innerchr11:106663950..106736815hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3872866
hg1972866
hg1872866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv783727
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556280
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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