A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029277



Internal ID18771809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152326306..152389689hg38UCSC Ensembl
Innerchr4:153247458..153310841hg19UCSC Ensembl
Innerchr4:153466908..153530291hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3863384
hg1963384
hg1863384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5440n100
Supporting Variantsnssv3636116, nssv3636117
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)nsv1029277
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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