A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv482915



Internal ID15582283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:32308555..32460333hg38UCSC Ensembl
Innerchr18:29888518..30040296hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38151779
hg19151779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996168, nssv2996211
Samples
Known GenesGAREM
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv482915
Frequency
Sample Size39
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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