A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556323



Internal ID16343732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107368667..107370321hg38UCSC Ensembl
Innerchr11:107239393..107241047hg19UCSC Ensembl
Innerchr11:106744603..106746257hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381655
hg191655
hg181655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2163n54
Supporting Variantsnssv784131
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556323
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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