A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556337



Internal ID16343746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107369080..107385214hg38UCSC Ensembl
Innerchr11:107239806..107255940hg19UCSC Ensembl
Innerchr11:106745016..106761150hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3816135
hg1916135
hg1816135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784155
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556337
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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