A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556359



Internal ID16343768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107370076..107372198hg38UCSC Ensembl
Innerchr11:107240802..107242924hg19UCSC Ensembl
Innerchr11:106746012..106748134hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg382123
hg192123
hg182123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2172n54
Supporting Variantsnssv784184
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556359
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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