A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv482983



Internal ID15582351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135404622..135555484hg38UCSC Ensembl
Innerchr7:135089374..135240232hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38150863
hg19150859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996324
Samples
Known GenesCNOT4
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv482983
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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