A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024767



Internal ID18767298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152321467..152387222hg38UCSC Ensembl
Innerchr4:153242619..153308374hg19UCSC Ensembl
Innerchr4:153462069..153527824hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3865756
hg1965756
hg1865756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5440n100
Supporting Variantsnssv3636104, nssv3636103
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)nsv1024767
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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