A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553995



Internal ID15994718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33111318..33455157hg38UCSC Ensembl
Innerchr11:33132864..33476703hg19UCSC Ensembl
Innerchr11:33089440..33433279hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38343840
hg19343840
hg18343840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1742n54
Supporting Variantsnssv771053
Samples
Known GenesCSTF3, CSTF3-AS1, HIPK3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553995
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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