A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555889



Internal ID16343298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90956309..91030944hg38UCSC Ensembl
Innerchr11:90689477..90764112hg19UCSC Ensembl
Innerchr11:90329125..90403760hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3874636
hg1974636
hg1874636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175392
SamplesHGDP00076
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555889
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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