A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483004



Internal ID15582372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:134894298..135073572hg38UCSC Ensembl
Innerchr8:135906541..136085815hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38179275
hg19179275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996138, nssv2996447
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483004
Frequency
Sample Size39
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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