A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552863



Internal ID15993586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:610277..618339hg38UCSC Ensembl
Innerchr11:610277..618339hg19UCSC Ensembl
Innerchr11:600277..608339hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg388063
hg198063
hg188063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1524n54
Supporting Variantsnssv763558
Samples
Known GenesCDHR5, IRF7, PHRF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552863
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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