A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555768



Internal ID15996491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89287330..89367161hg38UCSC Ensembl
Innerchr11:89020498..89100329hg19UCSC Ensembl
Innerchr11:88660146..88739977hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3879832
hg1979832
hg1879832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175389
SamplesHGDP00649
Known GenesNOX4, TYR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555768
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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