A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022314



Internal ID18764848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152321467..152364755hg38UCSC Ensembl
Innerchr4:153242619..153285907hg19UCSC Ensembl
Innerchr4:153462069..153505357hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3843289
hg1943289
hg1843289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5439n100
Supporting Variantsnssv3636100
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)nsv1022314
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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