A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552859



Internal ID15993582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:557342..656940hg38UCSC Ensembl
Innerchr11:557342..656940hg19UCSC Ensembl
Innerchr11:547342..646940hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3899599
hg1999599
hg1899599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1523n54
Supporting Variantsnssv763554
Samples
Known GenesC11orf35, CDHR5, DEAF1, DRD4, IRF7, LOC143666, MIR210, MIR210HG, PHRF1, RASSF7, SCT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552859
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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