A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483095



Internal ID15582208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34775701..34925104hg38UCSC Ensembl
Innerchr4:34777323..34926726hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38149404
hg19149404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996050, nssv2996532
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483095
Frequency
Sample Size39
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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