A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483107



Internal ID15582220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:106011489..106175832hg38UCSC Ensembl
Innerchr10:107771247..107935590hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38164344
hg19164344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996080
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483107
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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