A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483057



Internal ID15235531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72527446..72717131hg38UCSC Ensembl
Innerchr15:72819787..73009472hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38189686
hg19189686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996004, nssv2996061
Samples
Known GenesARIH1, BBS4, GOLGA6B, HIGD2B, MIR630
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483057
Frequency
Sample Size39
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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