A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556534



Internal ID16343943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:127318771..127328176hg38UCSC Ensembl
Innerchr11:127188666..127198071hg19UCSC Ensembl
Innerchr11:126693876..126703281hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg389406
hg199406
hg189406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784714
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556534
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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