A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483066



Internal ID15582179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:21765532..21900896hg38UCSC Ensembl
Innerchr21:23137852..23273216hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38135365
hg19135365
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996502
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483066
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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