A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555735



Internal ID15996458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89141912..89291287hg38UCSC Ensembl
Innerchr11:88875080..89024455hg19UCSC Ensembl
Innerchr11:88514728..88664103hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38149376
hg19149376
hg18149376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv780270
Samples
Known GenesTYR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555735
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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