A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483113



Internal ID15582226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:165903344..166066530hg38UCSC Ensembl
Innerchr5:165330349..165493535hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38163187
hg19163187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996341
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483113
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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