A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555941



Internal ID16343350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93396727..93447884hg38UCSC Ensembl
Innerchr11:93129893..93181050hg19UCSC Ensembl
Innerchr11:92769541..92820698hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3851158
hg1951158
hg1851158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781448
Samples
Known GenesCCDC67
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555941
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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