A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554409



Internal ID16341818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50372893..50807137hg38UCSC Ensembl
Innerchr11:50332064..50766308hg19UCSC Ensembl
Innerchr11:50288640..50722884hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38434245
hg19434245
hg18434245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1817n54
Supporting Variantsnssv773985, nssv773986
Samples
Known GenesLOC646813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554409
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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