A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv766307



Internal ID16060263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6094808..6097153hg38UCSC Ensembl
Innerchr11:6116038..6118383hg19UCSC Ensembl
Innerchr11:6072614..6074959hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382346
hg192346
hg182346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553354
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv766307
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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