A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556292



Internal ID16343701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107368380..107370321hg38UCSC Ensembl
Innerchr11:107239106..107241047hg19UCSC Ensembl
Innerchr11:106744316..106746257hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381942
hg191942
hg181942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2164n54
Supporting Variantsnssv783754, nssv783753
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556292
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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