A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv482919



Internal ID15582287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161813482..161986814hg38UCSC Ensembl
Innerchr4:162734634..162907966hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38173333
hg19173333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996461
Samples
Known GenesFSTL5
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv482919
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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