A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483011



Internal ID15582124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:103437775..103576897hg38UCSC Ensembl
Innerchr4:104358932..104498054hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38139123
hg19139123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996492
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483011
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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