A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556353



Internal ID16343762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107369763..107371425hg38UCSC Ensembl
Innerchr11:107240489..107242151hg19UCSC Ensembl
Innerchr11:106745699..106747361hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381663
hg191663
hg181663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2171n54
Supporting Variantsnssv784178
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556353
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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