A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555667



Internal ID16343076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86571638..86575359hg38UCSC Ensembl
Innerchr11:86282680..86286401hg19UCSC Ensembl
Innerchr11:85960328..85964049hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg383722
hg193722
hg183722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2046n54
Supporting Variantsnssv779963
Samples
Known GenesME3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555667
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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