A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv783754



Internal ID16077710
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 StatusS
Merged Variantsnsv556292
Supporting Variants
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv783754
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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