A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555326



Internal ID15996049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69651969..69654984hg38UCSC Ensembl
Innerchr11:69466737..69469752hg19UCSC Ensembl
Innerchr11:69175918..69178933hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg383016
hg193016
hg183016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv778760
Samples
Known GenesCCND1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555326
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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