A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028139



Internal ID18770670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152321467..152378692hg38UCSC Ensembl
Innerchr4:153242619..153299844hg19UCSC Ensembl
Innerchr4:153462069..153519294hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3857226
hg1957226
hg1857226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5440n100
Supporting Variantsnssv3636101
Samples
Known GenesDEAR, FBXW7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028139
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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