A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553234



Internal ID16340643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5361541..5362548hg38UCSC Ensembl
Innerchr11:5382771..5383778hg19UCSC Ensembl
Innerchr11:5339347..5340354hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381008
hg191008
hg181008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1598n54
Supporting Variantsnssv765358
Samples
Known GenesOR51B5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553234
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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