A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555220



Internal ID16342629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65874970..65875616hg38UCSC Ensembl
Innerchr11:65642441..65643087hg19UCSC Ensembl
Innerchr11:65399017..65399663hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38647
hg19647
hg18647
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1970n54
Supporting Variantsnssv778079, nssv778081, nssv778078, nssv778076, nssv778077, nssv778080
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555220
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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