A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv482981



Internal ID15235455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56833324..56982989hg38UCSC Ensembl
Innerchr11:56600800..56750464hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38149666
hg19149665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996295, nssv2996131
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv482981
Frequency
Sample Size39
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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