A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553314



Internal ID16340723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5760659..5783176hg38UCSC Ensembl
Innerchr11:5781889..5804406hg19UCSC Ensembl
Innerchr11:5738465..5760982hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3822518
hg1922518
hg1822518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1617n54
Supporting Variantsnssv765911
Samples
Known GenesOR52N5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553314
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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