A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556167



Internal ID16343576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:103118231..103185951hg38UCSC Ensembl
Innerchr11:102988960..103056680hg19UCSC Ensembl
Innerchr11:102494170..102561890hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3867721
hg1967721
hg1867721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2139n54
Supporting Variantsnssv1174952
SamplesHGDP01061
Known GenesDYNC2H1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556167
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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