A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553556



Internal ID15994279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14358520..14359205hg38UCSC Ensembl
Innerchr11:14380066..14380751hg19UCSC Ensembl
Innerchr11:14336642..14337327hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38686
hg19686
hg18686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1660n54
Supporting Variantsnssv768264
Samples
Known GenesRRAS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553556
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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