A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556485



Internal ID16343894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:123673197..123686888hg38UCSC Ensembl
Innerchr11:123543905..123557596hg19UCSC Ensembl
Innerchr11:123049115..123062806hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3813692
hg1913692
hg1813692
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784647
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556485
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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