A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016489



Internal ID18759024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152324311..152357705hg38UCSC Ensembl
Innerchr4:153245463..153278857hg19UCSC Ensembl
Innerchr4:153464913..153498307hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3833395
hg1933395
hg1833395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5439n100
Supporting Variantsnssv3636111
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)nsv1016489
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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