A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483079



Internal ID15582192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:11070537..11247630hg38UCSC Ensembl
Innerchr5:11070649..11247742hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38177094
hg19177094
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2995910
Samples
Known GenesCTNND2
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483079
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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