A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556010



Internal ID16343419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97866007..98472908hg38UCSC Ensembl
Innerchr11:97737007..98343637hg19UCSC Ensembl
Innerchr11:97242217..97848847hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38606902
hg19606631
hg18606631
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174915
Samples1780862111_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556010
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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