A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483089



Internal ID15582202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87069019..87216133hg38UCSC Ensembl
Innerchr15:87612250..87759364hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38147115
hg19147115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996167, nssv2996466
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483089
Frequency
Sample Size39
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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