A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553559



Internal ID15994282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14358571..14359268hg38UCSC Ensembl
Innerchr11:14380117..14380814hg19UCSC Ensembl
Innerchr11:14336693..14337390hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38698
hg19698
hg18698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1660n54
Supporting Variantsnssv768273
Samples
Known GenesRRAS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553559
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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