A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553284



Internal ID16340693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5738876..5740531hg38UCSC Ensembl
Innerchr11:5760106..5761761hg19UCSC Ensembl
Innerchr11:5716682..5718337hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381656
hg191656
hg181656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1610n54
Supporting Variantsnssv765585, nssv765584
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553284
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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