A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553337



Internal ID16340746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5768038..5787123hg38UCSC Ensembl
Innerchr11:5789268..5808353hg19UCSC Ensembl
Innerchr11:5745844..5764929hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3819086
hg1919086
hg1819086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1620n54
Supporting Variantsnssv766266, nssv766265, nssv766267
Samples
Known GenesOR52N5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553337
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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