A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483106



Internal ID15582219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:140061833..140239923hg38UCSC Ensembl
Innerchr3:139780675..139958765hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38178091
hg19178091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2995943
Samples
Known GenesCLSTN2
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483106
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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