A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556283



Internal ID16343692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107352178..107369524hg38UCSC Ensembl
Innerchr11:107222904..107240250hg19UCSC Ensembl
Innerchr11:106728114..106745460hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3817347
hg1917347
hg1817347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv783730
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556283
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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