A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556219



Internal ID15996942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:105004534..105047790hg38UCSC Ensembl
Innerchr11:104875261..104918517hg19UCSC Ensembl
Innerchr11:104380471..104423727hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3843257
hg1943257
hg1843257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv783374
Samples
Known GenesCARD16, CASP1, CASP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556219
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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