A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017089



Internal ID19106306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152326788..152413464hg38UCSC Ensembl
Innerchr4:153247940..153334616hg19UCSC Ensembl
Innerchr4:153467390..153554066hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3886677
hg1986677
hg1886677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5441n100
Supporting Variantsnssv3636121
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)nsv1017089
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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